Biaryl compounds as serine protease inhibitors

ABSTRACT

Compounds of formula (I) are useful as inhibitors of trypsin like serine protease enzymes such as thrombin, factor VIIa, factor Xa, TF/FVIIa, and trypsin. These compounds could be useful to treat and/or prevent clotting disorders, and as anticoagulating agents.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of copending International Patent Application No. PCT/US01/32582 filed Oct. 22, 2001, which designated the United States and which claims priority from U.S. patent application Ser. No. 60/281,735 filed Apr. 6, 2001, the disclosure of which is incorporated herein by reference.

TECHNICAL FIELD

The present invention relates to the identification, through synthesis and testing, of heretofore unreported compounds which, in appropriate pharmaceutical compositions, exert a therapeutic effect through reversible inhibition of serine proteases.

BACKGROUND OF INVENTION

Serine proteases make up the largest and most extensively studied group of proteolytic enzymes. Their critical roles in physiological processes extend over such diverse areas as blood coagulation, fibrinolysis, complement activation, reproduction, digestion, and the release of physiologically active peptides. Many of these vital processes begin with cleavage of a single peptide bond or a few peptide bonds in precursor protein or peptides. Sequential limited proteolytic reactions or cascades are involved in blood clotting, fibrinolysis, and complement activation. The biological signals to start these cascades can be controlled and amplified as well. Similarly, controlled proteolysis can shut down or inactivate proteins or peptides through single bond cleavages.

While serine proteases are physiologically vital, they also can be hazardous. Their proteolytic action, if uncontrolled, can destroy cells and tissues through degradation of proteins. As a natural safeguard in normal plasma, 10% of the protein matter is composed of protease inhibitors. The major natural plasma inhibitors are specific for serine proteinases. Diseases (associated protease given in the parentheses) such as pulmonary emphysema (cathepsin G), adult respiratory distress syndrome (chymases), and pancreatitis (trypsin, chymotrypsin, and others) are characterized by uncontrolled serine proteases. Other proteases appear to be involved in tumor invasion (plasmin, plasminogen activator), viral transformation, and inflammation (kallikrein). Thus the design and synthesis of specific inhibitors for this class of proteinases could offer major therapeutic benefits.

Thrombus formation, that is blood coagulation, is normally initiated by tissue injury; its normal purpose is to slow or prevent blood loss and facilitate wound healing. There are other conditions, however, not directly connected with tissue injury that may promote the coagulation process and lead instead to harmful consequences; examples of such conditions are atherosclerosis and inflammation.

The complex pathways of blood coagulation involve a series of enzyme reactions in which plasma coagulation factors, actually enzyme precursors or zymogens, are sequentially activated by limited proteolysis. Blood coagulation, or the coagulation cascade, is viewed mechanistically as two pathways, the extrinsic and the intrinsic (FIG. 1). Each pathway proceeds through a sequence of the Roman-numeral-designated factors until they converge at the activation of factor X after merger of the pathways. Thrombin generation proceeds stepwise through a common pathway. Thrombin then acts on the solution plasma protein, fibrinogen, to convert it to stable insoluble fibrin clots, thus completing the coagulation cascade.

The extrinsic pathway is vital to the initiation phase of blood coagulation while the intrinsic pathway provides necessary factors in the maintenance and growth of fibrin. The initiation of the coagulation cascade involves the release of tissue factor (TF) from injured vessel endothelial cells and subendothelium. TF then acts upon factor VII to form the TF/FVIIa complex (where VIIa designates the activated factor rather than the zymogen form). This complex initiates coagulation by activating factors IX and X. The resulting factor Xa forms a prothrombinase complex that activates prothrombin to produce the thrombin that converts fibrinogen to insoluble fibrin. In contrast, the intrinsic system is activated in vivo when certain coagulation proteins contact subendothelial connective tissue. In the sequence that follows, contact factors XII and XI are activated. The resulting factor XIa activates factor IX; then factor IXa activates factor X thereby intersecting with the extrinsic pathway.

With time, the TF/FVIIIa complex (of the extrinsic pathway) loses activity due to the action of tissue factor pathway inhibitor (TFPI), a Kunitz-type protease inhibitor protein which, when complexed with factor Xa, can inhibit the proteolytic activity of TF/FVIIa. If the extrinsic system is inhibited, additional factor Xa is produced through the thrombin-mediated action in the intrinsic pathway. Thrombin, therefore, exerts a dual catalytic role in (a) the conversion of fibrinogen to fibrin and (b) mediating its own production. The autocatalytic aspect of thrombin production affords an important safeguard against excessive blood loss, and, assuming presence of a threshold level of prothrombinase, ensures that the blood coagulation process will go to completion.

While the ability to form blood clots is vital to survival, there are disease states wherein the formation of blood clots within the circulatory system can cause death. When patients are afflicted with such disease states, it is not desirable to completely inhibit the clotting system because life-threatening hemorrhage would follow. Thus, it is highly desirable to develop agents that inhibit coagulation by inhibition of factor VIIa without directly inhibiting thrombin.

Need for the prevention of intravascular blood clots or for anti-coagulant treatment in many clinical situations is well known. Drugs in use today are often not satisfactory. A high percentage of patients who suffer internal injuries or undergo certain surgical procedures develop intravascular blood clots which, if unchecked, cause death. In total hip replacement surgery, for example, it is reported that 50% of the patients develop deep vein thrombosis (DVT). Current approved therapies involve administration of heparin in various forms, but results are not entirely satisfactory; 10-20% of patients suffer DVT and 5-10% have bleeding complications. Along these lines, see International Publication No. WO 00/15658.

Other examples of clinical situations for which better anticoagulants would be of great value are when patients undergo transluminal coronary angioplasty and treatment for myocardial infarction or crescendo angina. The present therapy for these conditions is administration of heparin and aspirin, but this treatment is associated with a 6-8% abrupt vessel closure rate within 24 hours of the procedure. Transfusion therapy due to bleeding complications is required in approximately 7% of cases following the use of heparin. Occurrences of delayed vessel closures are also significant, but administration of heparin after termination of the procedure affords little beneficial effect and can be detrimental.

Heparin and certain derivatives thereof are the most commonly used anti-clotting agents. These substances exert their effects mainly through inactivation of thrombin, which is inactivated 100 times faster than factor Xa. Two other thrombin-specific anticoagulants, hirudin and hirulog, are in clinical trials (as of September 1999). However, bleeding complications are associated with these agents.

In preclinical studies in baboons and dogs, the targeting of enzymes involved in earlier stages of the coagulation cascade, such as factor VIIa or factor Xa, prevents clot formation and does not produce bleeding side effects observed with direct thrombin inhibitors.

Several preclinical studies reveal that inhibition of TF/FVIIa offers the widest window of therapeutic effectiveness and safety with respect to bleeding risk of any anticoagulant approach tested including thrombin, platelet, and factor Xa inhibition.

A specific inhibitor of factor VIIa would provide clinicians with a valuable and needed agent that would be safe and effective in situations where the present drugs of choice, heparin and related sulfated polysaccharides, are no better than marginally effective.

There exists a need for a low molecular weight specific serine protease inhibitors specific toward various enzymes, particularly for factor VIIa that does not cause unwanted side effects.

The FIGURE illustrates the extrinsic and intrinsic pathways of blood coagulation.

SUMMARY OF INVENTION

An aspect of the present invention relates to compounds represented by the formula:

Each E¹ and L individually is a 5 to 7 membered saturated or unsaturated carbon ring, 5 to 7 membered saturated or unsaturated hetero ring, bicyclic saturated or unsaturated carbon ring, bicyclic saturated or unsaturated hetero ring, or 1-8 hydrocarbon chain which may be substituted with one or more hetero groups selected from N, O, S, S(O), and S(O₂) which may be saturated or unsaturated. The bicyclic rings typically contain 7-13 atoms in the ring.

R is —CH═CH—R², —C═C—R², —C(R²)═CH₂, —C(R²)═C(R³), —CH═NR², —C(R²)═N—R³, 4-7 membered saturated or unsaturated carbon ring system with or without substitution, 4-7 membered saturated or unsaturated hetero ring system with or without substitution, or chain of 2 to 8 carbon atoms having 1 to 5 double or triple bonds with substitutions selected from R¹, R², or R³.

R¹ is H, —R, —NO₂, —CN, -halo, —N₃, —C₁₋₈ alkyl, —(CH₂)_(n)CO₂R², —C₂₋₈ alkenyl-CO₂R², —O(CH₂)_(n)CO₂R², —C(O)NR²R³, —P(O)(OR²)₂, alkyl substituted tetrazol-5-yl —(CH₂)_(n)O(CH₂)_(n)aryl, —NR²R³, —(CH₂)_(n)OR², —(CH₂)_(n)SR², —N(R²)C(O)R³, —S(O₂)NR²R³, —N(R²)S(O₂)R³, —(CHR²)_(n)NR²R³, —C(O)R³, (CH₂)_(n)N(R³)C(O)R³, —N(R²)CR²R³ substituted or unsubstituted (CH₂)_(n)-cycloalkyl, substituted or unsubstituted (CH₂)_(n)-phenyl, or substituted or unsubstituted (CH₂)_(n)-heterocycle which may be saturated or unsaturated.

m is 1 except that when E¹ is a cyclic ring of more than 5 atoms, then m is 1 or higher, depending upon the size of the ring.

R² is H, -halo, -alkyl, -haloalkyl, —(CH₂)_(n)-phenyl, —(CH₂)₁₋₃-biphenyl, —(CH₂)₁₋₄—Ph—N(SO₂—C₁₋₂-alkyl)₂, —CO(CHR¹)_(n)—OR¹, —(CHR¹)_(n)-heterocycle, —(CHR¹)_(n)—NH—CO—R¹, —(CHR¹)_(n)—NH—SO₂R¹, —(CHR¹)_(n)—Ph—N(SO₂—C₁₋₂-alkyl)₂, —(CHR¹)_(n)—C(O)(CHR¹)—NHR¹, —(CHR¹)_(n)—C(S)(CHR¹)—NHR¹, —(CH₂)_(n)O(CH₂)_(n)CH₃, —CF₃, —C₂₋₅ acyl, —(CHR¹)_(n)OH, —(CHR¹)_(n)CO₂R¹, —(CHR¹)_(n)—O-alkyl, —(CHR¹)_(n)—O—(CH₂)_(n)—O-alkyl, —(CHR¹)_(n)—S-alkyl, —(CHR¹)_(n)—S(O)-alkyl, —(CHR¹)_(n)—S(O₂)-alkyl, —(CHR¹)_(n)—S(O₂)—NHR³, —(CHR³)_(n)—N₃, —(CHR³)_(n)NHR⁴, 2 to 8 carbon atom alkene chain having 1 to 5 double bonds, 2 to 8 carbon atom alkyne chain having 1 to 5 triple bonds, substituted or unsubstituted-(CHR³)_(n) heterocycle, or substituted or unsubstituted-(CHR³)_(n) cycloalkyl which may be saturated or unsaturated.

When n is more than 1, the substitutions R¹ and R³ may be same or different.

R³ is H, —OH, —CN, substituted alkyl, —C₂₋₈ alkenyl, substituted or unsubstituted cycloalkyl, —N(R¹)R², or 5-6 membered saturated substituted or unsubstituted hetero ring.

—NR²R³ may form a ring system having 4 to 7 atoms or may be bicyclic ring. The ring system may be of carbon or hetero atoms and further it may saturated or unsaturated and also may be substituted or unsubstituted.

W is a direct bond, —CHR²—, —CH═CR²—, —CR═CH—, —CR²═CR²—, —C═C—, —O—CHR²—, —CHR²—O—, —N(R²)—C(O)—, —C(O)—N(R²)—, —N(R²)—CH—(R³)—, —CH₂—N(R²)—, —CH(R¹)—N(R²)—, —S—CHR²—, —CHR²—S—, —S(O₂)—N(R²)—, —C(O)N(R²)—(CHR²)_(n)—, —C(R¹R²)_(n)—NR²—, —N(R²)—S(O₂)—, —R²C(O)NR²—, —R²NC(O)NR²—, —CONR²CO—, —C(═NR²)NR²—, —NR²C(═NR²)NR²—, —NR²O—, —N═NCHR²—, or —C(O)NR²SO₂—.

E² is 5 to 7 membered saturated or unsaturated carbon ring, 5 to 7 membered saturated or unsaturated hetero ring, bicyclic ring system, C₁₋₈ alkyl, C₂₋₈ alkenyl, C₂₋₈ alkynyl, alkylaryl, aralkyl, aralkenyl, aralkynyl, alkoxy, alkylthio, or alkylamino.

each X individually is a direct bond, substituted or unsubstituted C₁₋₄ methylene chain; O, S, NR², S(O), S(O₂), or N(O) containing one or two C₁₋₄ substituted or unsubstituted methylene chains. X at different places may be same or different.

B is H, -halo, —CN, —NH₂, —(CH₂)_(n)—C(═NR⁴)NHR⁵, —(CH₂)_(n)—NHR⁴, —(CH₂)_(n)NHC(═NR⁴)NR⁵, —(CH₂)_(n)—OR⁴, C₁₋₈ substituted or unsubstituted alkyl, substituted or unsubstituted ring system having 4 to 7 carbon or hetero atoms which may be saturated or unsaturated.

B¹ is selected from B; B¹ and B may be same or different.

There may be more than one similar or different R² groups present on E², when E² is a cyclic group of more than 5 atoms. In particular, p is 1 except that when E² is a cyclic ring of more than 5 atoms, p is 1 or higher depending upon the size of the ring.

n is 0-4

A is selected from R¹.

o is 1 except that when L is a cyclic ring of more than 5 atoms, o is 1 or higher depending upon the size of the ring.

Each V and V¹ individually is selected from R¹ and N-alkyl substituted carboxamidyl (—CONHR) where the alkyl group may be straight, branched, cyclic, or bicyclic; N,N-disubstituted carboxamidyl (—CONR₁R₂ where R₁ and R₂ may be substituted or unsubstituted alkyl or aryl and may be the same or different); mono- or disubstituted sulfonamides (SO₂NHR or —SO₂NR₁R₂); and methylene- or polymethylene chain-extended variants thereof.

Each R⁴ and R⁵ individually is H, —(CH₂)_(n)OH, —C(O)OR⁶, —C(O)SR⁶, —(CH₂)_(n)C(O)NR⁷R⁸, —O—C(O)—O—R⁷, an amino acid or a dipeptide,

Each R⁶ is H, R⁷, —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—R⁹, —(CH₂)_(n)—C(R⁷)(R⁸)—O—C(O)R⁹, —(CH₂)_(n)—C(R⁷)(R⁸)—O—C(O)—O—R⁹, or —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—O—R⁹,

Each R⁷, R⁸ and R⁹ individually is H, alkyl, substituted alkyl, aryl, substituted aryl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, heterocycle, substituted heterocycle, alkylaryl, substituted alkylaryl, cycloalkyl, substituted cycloalkyl, or CH₂CO₂alkyl.

The present invention also relates to pharmaceutical compositions containing at least one of the above disclosed compounds and their prodrugs.

A further aspect of the present invention relates to a method for inhibiting trypsin-like serine protease enzymes, such as thrombin, factor Xa, factor VIIa, TF/VIIa, and trypsin in a patient which comprises administering to the patient an effective serine protease inhibiting amount of at least one of the above disclosed compounds.

Still other objects and advantages of the present invention will become readily apparent by those skilled in the art from the following detailed description, wherein it is shown and described preferred embodiments of the invention, simply by way of illustration of the best mode contemplated of carrying out the invention. As will be realized the invention is capable of other and different embodiments, and its several details are capable of modifications in various obvious respects, without departing from the invention. Accordingly, the description is to be regarded as illustrative in nature and not as restrictive.

BEST AND VARIOUS MODES FOR CARRYING OUT INVENTION

An aspect of the present invention relates to compounds represented by the formula:

Each E¹ and L individually is a 5 to 7 membered saturated or unsaturated carbon ring, 5 to 7 membered saturated or unsaturated hetero ring, bicyclic saturated or unsaturated carbon ring, bicyclic saturated or unsaturated hetero ring, or 1-8 hydrocarbon chain which may be substituted with one or more hetero groups selected from N, O, S, S(O), and S(O₂) which may be saturated or unsaturated.

R is —CH═CH—R², —C═C—R², —C(R²)═CH₂, —C(R²)═C(R³), —CH═NR², —C(R²)═N—R³, 4-7 membered saturated or unsaturated carbon ring system with or without substitution, 4-7 membered saturated or unsaturated hetero ring system with or without substitution, or chain of 2 to 8 carbon atoms having 1 to 5 double or triple bonds with substitutions selected from R¹, R², or R³. Preferably, these R, R¹, R², or R³ do not include —C₂₋₄ alkenyl)-CO₂—C₁₋₈ alkyl, —(C₂₋₄ alkenyl)-CO₂—C₁₋₈ alkyl-phenyl, and —(C₂₋₄ alkenyl)-CO₂—C₁₋₈ alkyl-O—C₁₋₄ alkyl.

R¹ is H, —R, —NO₂, —CN, -halo, —N₃, —C₁₋₈ alkyl, —(CH₂)_(n)CO₂R², —C₂₋₈ alkenyl-CO₂R², —O(CH₂)_(n)CO₂R², —C(O)NR²R³, —P(O)(OR²)₂, alkyl substituted tetrazol-5-yl, —(CH₂)_(n)O(CH₂)_(n)aryl, —NR²R³, —(CH₂)_(n)OR², —(CH₂)_(n)SR², —N(R²)C(O)R³, —S(O₂)NR²R³, —N(R²)S(O₂)R³, —(CHR²)_(n)NR²R³, —C(O)R³, (CH₂)_(n)N(R³)C(O)R³, —N(R²)CR²R³ substituted or unsubstituted (CH₂)_(n)-cycloalkyl, substituted or unsubstituted (CH₂)_(n)-phenyl, or substituted or unsubstituted (CH₂)_(n)-heterocycle which may be saturated or unsaturated.

m is 1 except that when E¹ is a cyclic ring of more than 5 atoms, then m is 1 or higher, depending upon the size of the ring. For instance if the ring is 6 atoms, m can be 1 or 2.

R² is H, -halo, -alkyl, -haloalkyl, —(CH₂)_(n)-phenyl, —(CH₂)₁₋₃-biphenyl, —(CH₂)₁₋₄—Ph—N(SO₂—C₁₋₂-alkyl)₂, —CO(CHR¹)_(n)—OR¹, —(CHR¹)_(n)-heterocycle, —(CHR¹)_(n)—NH—CO—R¹, —(CHR¹)_(n)—NH—SO₂R¹, —(CHR¹)_(n)—Ph—N(SO₂—C₁₋₂-alkyl)₂, —(CHR¹)_(n)—C(O)(CHR¹)—NHR¹, —(CHR¹)_(n)—C(S)(CHR¹)—NHR¹, —(CH₂)_(n)O(CH₂)_(n)CH₃, —CF₃, —C₂₋₅ acyl, —(CHR¹)_(n)OH, —(CHR¹)_(n)CO₂R¹, —(CHR¹)_(n)—O-alkyl, —(CHR¹)_(n)—O—(CH₂)_(n)—O-alkyl, —(CHR¹)_(n)—S-alkyl, —(CHR¹)_(n)—S(O)-alkyl, —(CHR¹)_(n)—S(O₂)-alkyl, —(CHR¹)_(n)—S(O₂)—NHR³, —(CHR³)_(n)—N₃, —(CHR³)_(n)NHR⁴, 2 to 8 carbon atom alkene chain having 1 to 5 double bonds, 2 to 8 carbon atom alkyne chain having 1 to 5 triple bonds, substituted or unsubstituted-(CHR³)_(n) heterocycle, or substituted or unsubstituted-(CHR³)_(n) cycloalkyl which may be saturated or unsaturated.

When n is more than 1, the substitutions R¹ and R³ may be same or different.

R³ is H, —OH, —CN, substituted alkyl, —C₂₋₈ alkenyl, substituted or unsubstituted cycloalkyl, —N(R¹)R², or 5-6 membered saturated substituted or unsubstituted hetero ring.

—NR²R³ may form a ring system having 4 to 7 atoms or may be bicyclic ring. The ring system may be of carbon or hetero atoms and further it may saturated or unsaturated and also may be substituted or unsubstituted.

W is a direct bond, —CHR²—, —CH═CR²—, —CR═CH—, —CR²═CR²—, —C═C—, —O—CHR²—, —CHR²—O—, —N(R²)—C(O)—, —C(O)—N(R²)—, —N(R²)—CH—(R³)—, —CH₂—N(R²)—, —CH(R¹)—N(R²)—, —S—CHR—, —CHR²—S—, —S(O₂)—N(R²)—, —C(O)N(R²)—(CHR²)_(n)—, —C(R¹R²)_(n)—NR²—, —N(R²)—S(O₂)—, —R²C(O)NR²—, —R²NC(O)NR²—, —CONR²CO—, —C(═NR²)NR²—, —NR²C(═NR²)NR²—, —NR²O, —N═NCHR²—, or —C(O)NR²SO₂—.

E² is 5 to 7 membered saturated or unsaturated carbon ring, 5 to 7 membered saturated or unsaturated hetero ring, bicyclic ring system, C₁₋₈ alkyl, C₂₋₈ alkenyl, C₂₋₈ alkynyl, alkylaryl, aralkyl, aralkenyl, aralkynyl, alkoxy, alkylthio, or alkylamino.

each X individually is a direct bond, substituted or unsubstituted C₁₋₄ methylene chain; O, S, NR², S(O), S(O₂), or N(O) containing one or two C₁₋₄ substituted or unsubstituted methylene chains. X at different places may be same or different.

B is H, -halo, —CN, —NH₂, —(CH₂)_(n)—C(═NR⁴)NHR⁵, —(CH₂)_(n)—NHR⁴, —(CH₂)_(n)NHC(═NR⁴)NR⁵, —(CH₂)_(n)—OR⁴, C₁₋₈ substituted or unsubstituted alkyl, substituted or unsubstituted ring system having 4 to 7 carbon or hetero atoms which may be saturated or unsaturated.

B¹ is selected from B; B¹ and B may be same or different.

There may be more than one similar or different R² groups present on E², when E² is a cyclic system of more than 5 atoms. p is 1 or higher if E² is a cyclic ring of more than 5 atoms. For example, if the ring is 6 atoms, p can be 1 or 2.

n is 0-4

A is selected from R¹.

o is 1 except that when L is a cyclic ring of more than 5 atoms, o is 1 or higher depending upon the size of the ring. For instance, if the ring is 6 atoms, o can be 1 or 2.

Each V and V¹ individually is selected from R¹ and N-alkyl substituted carboxamidyl (—CONHR) where the alkyl group may be straight, branched, cyclic, or bicyclic; N,N-disubstituted carboxamidyl (—CONR₁R₂ where R₁ and R₂ may be substituted or unsubstituted alkyl or aryl and may be the same or different); mono- or disubstituted sulfonamides (SO₂NHR or —SO₂NR₁R₂); and methylene- or polymethylene chain-extended variants thereof.

Each R⁴ and R⁵ individually is H, —(CH₂)_(n)OH, —C(O)OR⁶, —C(O)SR⁶, —(CH₂)_(n)C(O)NR⁷R⁸, —O—C(O)—O—R⁷, an amino acid or a dipeptide,

Each R⁶ is H, R⁷, —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—R⁹, —(CH₂)_(n—C(R) ⁷)(R⁸)—O—C(O)R⁹, —(CH₂)_(n)—C(R⁷)(R⁸)—O—C(O)—O—R⁹, or —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—O—R⁹,

Each R⁷, R⁸ and R⁹ individually is H, alkyl, substituted alkyl, aryl, substituted aryl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, heterocycle, substituted heterocycle, alkylaryl, substituted alkylaryl, cycloalkyl, substituted cycloalkyl, or CH₂CO₂alkyl.

R substituent groups employed pursuant to the present invention contribute to significantly enhanced activity of the compounds of the present invention.

Listed below are definitions of various terms used to describe this invention. These definitions apply to the terms as they are used throughout this specification, unless otherwise limited in specific instances, either individually or as part of a larger group.

The term “alkyl” refers to straight or branched chain unsubstituted hydrocarbon groups of 1 to 20 carbon atoms, preferably 1 to 8 carbon atoms. The expression “lower alkyl” refers to unsubstituted alkyl groups of 1 to 4 carbon atoms.

The terms “alkenyl” and “alkynyl” refer to straight or branched chain unsubstituted hydrocarbon groups typically having 2 to 8 carbon atoms.

The terms “substituted alkyl”, “substituted alkenyl” or substituted alkynyl” refer to an alkyl, alkenyl or alkynyl group substituted by, for example, one to four substituents, such as halo, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cycloalkyloxy, heterocyclooxy, oxo, alkanoyl, aryloxy, alkanoyloxy, amino, alkylamino, arylamino, aralkylamino, cycloalkylamino, heterocycloamino, disubstituted amines in which the 2 amino substituents are selected from alkyl, aryl or aralkyl, alkanoylamine, aroylamino, aralkanoylamino, substituted alkanolamino, substituted arylamino, substituted aralkanoylamino, thiol, alkylthio, arylthio, aralkylthio, cycloalkylthio, heterocyclothio, alkylthiono, arylthiono, aralkylthiono, alkylsulfonyl, arylsulfonyl, aralkylsulfonyl, sulfonamido (e.g. SO₂NH₂), substituted sulfonamido, nitro, cyano, carboxy, carbamyl (e.g. CONH₂), substituted carbamyl (e.g. CONH alkyl, CONH aryl, CONH aralkyl or cases where there are two substituents on the nitrogen selected from alkyl, aryl or aralkyl), alkoxycarbonyl, aryl, substituted aryl, guanidino and heterocyclos, such as indolyl, imidazolyl, furyl, thienyl, thiazolyl, pyrrolidyl, pyridyl, pyrimidyl and the like. Where noted above where the substituent is further substituted it will be with halogen, alkyl, alkoxy, aryl or aralkyl.

The term “halogen” or “halo” refers to fluorine, chlorine, bromine and iodine.

The term “aryl” refers to monocyclic or bicyclic aromatic hydrocarbon groups having 6 to 12 carbon atoms in the ring portion, such as phenyl, naphthyl, biphenyl and diphenyl groups, each of which may be substituted.

The term “aralkyl” or “alkylaryl” refers to an aryl group bonded directly through an alkyl group, such as benzyl or phenethyl.

The term “substituted aryl” or “substituted alkylaryl” refers to an aryl group or alkylaryl group substituted by, for example, one to four substituents such as alkyl; substituted alkyl, halo, trifluoromethoxy, trifluoromethyl, hydroxy, alkoxy, azido, cycloalkyloxy, heterocyclooxy, alkanoyl, alkanoyloxy, amino, alkylamino, aralkylamino, hydroxyalkyl, aminoalkyl, azidoalkyl, alkenyl, alkynyl, allenyl, cycloalkylamino, heterocycloamino, dialkylamino, alkanoylamino, thiol, alkylthio, cycloalkylthio, heterocyclothio, ureido, nitro, cyano, carboxy, carboxyalkyl, carbamyl, alkoxycarbonyl, alkylthiono, arylthiono, alkysulfonyl, sulfonamido, aryloxy and the like. The substituent may be further substituted by halo, hydroxy, alkyl, alkoxy, aryl, substituted aryl, substituted alkyl or aralkyl. “Substituted benzyl” refers to a benzyl group substituted by, for example, any of the groups listed above for substituted aryl.

The term “cycloalkyl” refers to optionally substituted, saturated cyclic hydrocarbon ring systems, preferably containing 1 to 3 rings and 3 to 7 carbons per ring which may be further fused with an unsaturated C₃-C₇ carbocyclic ring. Exemplary groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl, cyclododecyl and adamantyl. Exemplary substituents include one or more alkyl groups as described above, or one or more groups described above as alkyl substituents.

The term “cycloalkenyl” refers to optionally substituted, unsaturated cyclic hydrocarbon ring systems, preferably containing 1 to 3 rings and 3-7 carbons per ring. Exemplary groups include cyclopentenyl and cyclohexenyl.

The terms “heterocycle”, “heterocyclic” and “heterocyclo” refer to an optionally substituted, fully saturated or unsaturated, aromatic or nonaromatic cyclic group, for example, which is 4 to 7 membered monocyclic, 7 to 11 membered bicyclic, or 10 to 15 membered tricyclic ring system, which has at least one heteroatom in at least one carbon atom-containing ring. Each ring of the heterocyclic group containing a heteroatom may have 1, 2 or 3 heteroatoms selected from nitrogen atoms, oxygen atoms and sulfur atoms, where the nitrogen and sulfur heteroatoms may also optionally be oxidized and the nitrogen heteroatoms may also optionally be quaternized. The heterocyclic group may be attached at any heteroatom or carbon atoms.

Exemplary monocyclic heterocyclic groups include pyrrolidinyl, pyrrolyl, indolyl, pyrazolyl, oxetanyl, pyrazolinyl, imidazolyl, imidazolinyl, imidazolidinyl, oxazolyl, oxazolidinyl, isoxazolinyl, isoxazolyl, thiazolyl, thiadiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, furyl, tetrahydrofuryl, thienyl, thiophenyl, oxadiazolyl, piperidinyl, piperazinyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, 2-oxazepinyl, azepinyl, 4-piperidonyl, pyridyl, dihydropyridyl, N-oxo-pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydrothiopyranyl sulfone, morpholinyl, thiomorpholinyl, thiomorpholinyl sulfoxide, thiomorpholinyl sulfone, 1,3-dixolane and tetrahydro-1,1-dioxothienyl, dioxanyl, isothiazolidinyl, thietanyl, thiiranyl, triazinyl and triazolyl and the like.

Exemplary bicyclic heterocyclic groups include benzothiazolyl, benzoxazolyl, benzothienyl, quinuclidinyl, quinolinyl, quinolinyl-N-oxide, tetrahydroisoquinolinyl, isoquinolinyl, benzimidazolyl, benzopyranyl, indolizinyl, benzofuryl, chromonyl, coumarinyl, cinnolinyl, quinoxalinyl, indazolyl, pyrrolapridyl, furopyridinyl (such as furo[2,3-c]pyridinyl, furo[3,1-b]pyridinyl, or furo[2,3-b]pyridinyl), dihydroisoindolyl, diyhydroquinazolinyl (such as 3,4-dihydro-4-oxo-quinazolinyl), benzisothiazolyl, benzisoxazolyl, benzodiazinyl, benzofurazanyl, benzothiopyranyl, benzothiazolyl, benzpyrasolyl, dihydrobenzofuryl, dihydrobenzothienyl, dihydrobenzothiopyranyl, dihydrobenzothiopyranyl sulfone, dihydrobenzopyranyl, indolinyl, isochromanyl, isoindolinyl, naphthyridinyl, phthalazinyl, piperonyl, purinyl, pyridopyridyl, quinazolinyl, tetrahydroquinolinyl, theinofuryl, thienopyridyl, thienothienyl, and the like.

Exemplary substituents include one or more alkyl groups as described above or one or more groups described above as alkyl substituents.

Within the above-described definitions, certain embodiments are preferred. Preferred alkyl groups are lower alkyl groups containing 1 to about 8 carbon, and more preferably 1 to about 5 carbon atoms, and can be straight, branched-chain or cyclic saturated aliphatic hydrocarbon groups.

Examples of suitable alkyl groups include methyl, ethyl and propyl. Examples of branched alkyl groups include isopropyl and t-butyl. An example of a suitable alkylaryl group is phenethyl. Examples of suitable cycloalkyl groups typically contain 3-8 carbon atoms and include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. The aromatic or aryl groups are preferably phenyl or alkyl substituted aromatic groups (aralkyl) such as phenyl C₁₋₃ alkyl such as benzyl.

The N-heterocyclic rings preferably contain 3-7 atoms in the ring and a heteroatom such as N, S or O in the ring. Examples of suitable preferred heterocyclic groups are pyrrolidino, azetidino, piperidino, 3,4-didehydropiperidino, 2-methylpiperidino and 2-ethylpiperidino. In addition, the above substitutions can include halo such as F, Cl, Br, lower alkyl, lower alkoxy and halo substituted lower alkoxy.

Examples of some preferred B groups include —NHC(═NH)NH₂, —C(═NH)NH₂, NH₂, various N-substituted variants, and assorted prodrug derivatives.

Prodrug forms of the compounds bearing various nitrogen functions (amino, hydroxyamino, hydrazino, guanidino, amidino, amide, etc.) may include the following types of derivatives where each R group individually may be hydrogen, substituted or unsubstituted alkyl, aryl, alkenyl, alkynyl, heterocycle, alkylaryl, aralkyl, aralkenyl, aralkynyl, cycloalkyl, or cycloalkenyl groups as defined beginning on page 7.

(a) Carboxamides, —NHC(O)R

(b) Carbamates, —NHC(O)OR

(c) (Acyloxy)alkyl carbamates, —NHC(O)OROC(O)R

(d) Enamines, —NHCR(═CHCRO₂R) or —NHCR(═CHCRONR₂)

(e) Schiff bases, —N═CR₂

(f) Mannich bases (from carboximide compounds), RCONHCH₂NR₂

Preparations of such prodrug derivatives are discussed in various literature sources (examples are: Alexander et al., J. Med. Chem. 1988, 31, 318; Aligas-Martin et al., PCT WO pp/41531, p. 30). The nitrogen function converted in preparing these derivatives is one (or more) of the nitrogen atoms of a compound of the invention.

Prodrug forms of carboxyl-bearing compounds of the invention include esters (—CO₂R) where the R group corresponds to any alcohol whose release in the body through enzymatic or hydrolytic processes would be at pharmaceutically acceptable levels. Another prodrug derived from a carboxylic acid form of the invention may be a quaternary salt type

of structure described by Boder et al., J. Med. Chem. 1980, 23, 469.

Examples of some preferred groups for W are —CH₂CH₂—, —CH═CH—, —C≡C—, —CH₂CH₂CH₂—, —CH₂CH═CH—, —CH₂C≡C—, —CONH, —CH₂CONH—, —NHCONH—, —CONHCO—, —CONHCH₂—, —C(═NH)NH—, —CH₂C(═NH)NH—, —NHC(═NH)NH—, —NHNH—, —NHO—, —CONHSO₂—, —SO₂NH—, —NHSO₂CH₂—, —SO₂NHCH₂—, —CH₂O—, —CH₂OCH₂—, —OCH₂CH₂—, —CH₂NH—, —CH₂CH₂NH—, —CH₂NHCH₂—, —CH₂S—, —SCH₂CH₂, —CH₂SCH₂—, —CH₂SO₂CH₂—, —CH₂SOCH₂—, —CH(CO₂H)O and —CH(CO₂H)OCH₂.

Examples of some preferred groups for V and V¹ are N-alkyl substituted carboxamidyl (—CONHR) where the alkyl group may be straight, branched, cyclic, or bicyclic, and typically containing up to ten carbons; N,N-disubstituted carboxamidyl (—CONR₁R₂ where R₁ and R₂ may be substituted or unsubstituted alkyl or aryl and may be the same or different); mono- or disubstituted sulfonamides (SO₂NHR or —SO₂NR₁R₂); methylene- or polymethylene chain- extended variants thereof such as —CH₂)_(n)CONHR₁, —(CH₂)_(n)CONR₁R₂, —(CH₂)_(n)SO₂NHR₁, —(CH₂)_(n)SO₂NR₁R₂ (where n=1-4), —NHC(O)R, N(R₁)C(O)R₂, NHSO₂R, CH₂NHR, CH₂NR₁R₂.

Pharmaceutically acceptable salts of the compounds of the present invention include those derived from pharmaceutically acceptable, inorganic and organic acids and bases. Examples of suitable acids include hydrochloric, hydrobromic, sulphuric, nitric, perchloric, fumaric, maleic, phosphoric, glycollic, lactic, salicyclic, succinic, toluene-p-sulphonic, tartaric, acetic, citric, methanesulphonic, formic, benzoic, malonic, naphthalene-2-sulphonic, trifluoroacetic and benzenesulphonic acids.

Salts derived from appropriate bases include alkali such as sodium and ammonia.

It is of course understood that the compounds of the present invention relate to all optical isomers and stereo-isomers at the various possible atoms of the molecule.

The synthetic routes leading to the compounds in formula (I) are described in the following schemes.

Conversion of

The reduction of the formyl group of 24ab, 24ac, 24ae, and 24ad was accomplished with NaBH₄ to give corresponding alcohols 24ab-i, 24ac-i, 24ae-i, and 24ad-i, respectively. Later, the MEM group was removed under acidic conditions to give 25ab, 25ac, 25ae, and 25af, respectively.

Conversion of

The aldehyde 24ad was oxidized to acid 24ad-i which was protected as benzyl ester to give 24ad-ii. MEM deprotection under acidic conditions produced 25ad.

Conversion of

The vinyl compound 24ah was oxidized with OsO₄ to give diol 24ah-i, followed by acidic hydrolysis of the MEM group to produce 25ah.

Conversion of

The vinyl compound 24ah on dihydroxylation with OsO₄ gave diol 24ah-i. Oxidative cleavage of the diol with NalO₄ produced aldehyde 24ah-ii. The aldehyde on reduction gave alcohol 24ah-iii, which on further reaction with methane sulfonyl chloride yielded mesylate 24ah-iv. The mesylate on further reaction with sodium azide gave the corresponding azide 24ah-v, which on acidic hydrolysis produced 25ai.

Conversion of

Conversion of

Aldehyde 29g was converted to alcohol 29g-i by reduction with NaBH₄, followed by the reaction of methanesulfonyl chloride to give mesylate 29g-ii. The mesyl group was displaced with azide to give 29g-iii and finally, the MEM group was removed under acidic conditions to give 30g.

Conversion of

The reduction of the formyl group of 29h and 29i was accomplished with NaBH₄ to give corresponding alcohols 29h-i and 29i-i, respectively. Later, the MEM group was removed under acidic conditions to give 30h and 30i, respectively.

Compounds of the type 23 and 28, where X=—Sn(Bu)₃, are prepared using the methods AG-1 or AG-2

It was prepared the same way as 229 using propylamine in method A-3

GENERAL METHODS OF PREPARATION

The following abbreviations have been used:

THF: Tetrahydrofuran; DMF: Dimethylformamide

DME: 1,2-Dimethoxyethane; DMAP: 4-(Dimethylamino)pyridine

Boc anhydride: Di-tert-butyl dicarbonate; TIPS: Triisopropylsilyl

MEM: Methoxyethoxymethyl; Bn: Phenylmethyl or Benzyl

The organic extracts were dried over sodium sulfate or magnesium sulfate.

The general methods for the preparation of the compounds of formula (I) are given below:

A-1: Conversion of Acid to Amide

To derivative (1 mmol), was added thionyl chloride (12.6 mmol) and a few drops of DMF. The reaction mixture was refluxed for 2 h and concentrated in vacuo to obtain an oily residue. The residue was dissolved in dichloromethane (3 mL); cooled with ice water and amine (5 mmol) was added. The reaction mixture was stirred at room temperature overnight, washed with 1N HCl, saturated sodium hydrogen carbonate, water, brine, dried and concentrated in vacuo. The product obtained was purified by crystallization or flash column chromatography to furnish the desired amide.

A-2: Conversion of Acid to Amide

To a solution of acid derivative (1 mmol) in dichloromethane (10 mL) at 0° C. was added triethylamine (3 mmol) and ethyl chloroformate (3 mmol). The reaction mixture was stirred at the same temperature for 30 min and the corresponding amine (6 mmol) was added. The reaction mixture was stirred at room temperature overnight and quenched with 1N HCl. The organic layer was separated washed with water, brine, dried and concentrated in vacuo. The product obtained was purified by crystallization or flash column chromatography to furnish the desired amide.

A-3: Conversion of Acid to Amide

To a solution of acid (1 mmol) in dichloromethane (5 mL) was added 2M oxalyl chloride in dichloromethane (2.5 mmol), followed by a drop of DMF. The reaction mixture was stirred for 2 h at room temperature and concentrated in vacuo. The residue was co-evaporated once with dichloromethane (5 mL) and then dried in vacuo. To the residue in dichloromethane (10 mL) were further added triethylamine (3 mmol) and the corresponding amine (1.2 mmol). The reaction mixture was stirred for 16 h and washed with water, brine, dried and concentrated in vacuo. The product obtained was purified by crystallization or flash column chromatography to furnish the desired amide.

A-4: Conversion of Acid to Amide

To a solution of acid (1 mmol) in dichloromethane or THF (10 mL) cooled with an ice bath was added triethylamine (1.2 mmol) and ethyl chloroformate or isobutyl chloroformate (1.2 mmol). The reaction mixture was stirred at 0° C. for 30 min and the corresponding amine (2.5 mmol) was added. The reaction mixture was stirred at room temperature overnight and quenched with 1N HCl. The organic layer was separated, washed with water, brine, dried and concentrated in vacuo. The product obtained was purified by crystallization or flash column chromatography to furnish the desired amide.

A-5: Conversion of Acid to Amide

A mixture of carboxylic acid (1 mmol), amine (1.1 mmol), 1-hydroxybenzotriazole (1 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide (1.1 mmol) in pyridine (10 mL) was stirred overnight at room temperature and was concentrated in vacuo to dryness. The residue obtained was purified by column chromatography or used as such for the next step.

A-6: Reduction of Acid to Alcohol

To a solution of acid (1 mmol) in dichloromethane or THF (10 mL) at 0° C. was added triethylamine (1.2 mmol) and ethyl chloroformate or isobutyl chloroformate (1.2 mmol). The reaction mixture was stirred at 0° C. for 30 min and sodium borohydride (1.25 mmol) was added. The reaction mixture was stirred at room temperature overnight and quenched with 1N HCl. The reaction mixture was extracted with ethyl acetate. The organic layers were combined, washed with water, brine, dried and concentrated in vacuo to furnish the desired alcohol. This can be purified further, if needed, by crystallization or column chromatography.

A-7: Conversion of Acid to Amide

A mixture of carboxylic acid (1 mmol), amine (1 mmol), and 4-dimethylaminopyridie (0.12 mmol) in xylene (10 mL) was stirred at 80° C. for 10 min. Phosphorus trichloride (1 mmol) was added and the reaction mixture was heated with stirring at 150° C. for 2 hr. After cooling, the product was extracted with EtOAc. The organic layers were combined, washed with water, brine, dried and concentrated in vacuo. The product obtained was purified by flash column chromatography to furnish the desired amide.

B-1: Conversion of Phenolic Hydroxyl to Triflate

To a phenol (1 mmol) in dichloromethane (2.5 mL) was added pyridine (5 mmol) under a nitrogen atmosphere and cooled to −10 C. To the cold reaction mixture was added dropwise triflic anhydride (2 mmol) in dichloromethane (2.5 mL) over a period of 10 mins and allowed to warm to room temperature and stirred for 16 h. The reaction mixture was quenched with saturated aqueous sodium hydrogen carbonate solution and the organic layer was separated. The organic layer was washed with 1N HCl, saturated sodium hydrogen carbonate, water, brine, dried and concentrated in vacuo. The product obtained was purified by crystallization or flash column chromatography to furnish the desired triflate.

B-2: Conversion of Phenolic Hydroxyl to Triflate

To a solution of substituted phenol (1 mmol) in DMF (10 mL) was added N-phenylbis(trifluoromethanesulphonimide) (1.1 mmol), and triethylamine (2 mmol) and stirred at room temperature overnight. The reaction mixture was quenched with ice water and extracted twice with ether. The organic layers were combined, washed with brine, dried and concentrated in vacuo to furnish the desired triflate.

C: Conversion of Acid to MEM Ester

To a solution of acid derivative (1 mmol) in DMF (10 mL) was added sodium bicarbonate (1.05 mmol), and MEM-Cl (1.05 mmol) and was stirred at room temperature for 24 h. The reaction mixture was quenched with ice water and extracted twice with ether. The organic layers were combined, washed with brine, dried and concentrated in vacuo to furnish crude product. Purification by flash column chromatography or crystallization gave the desired MEM ester.

D-1: Coupling of Boronic Acid With Triflate

A mixture of triflate (1 mmol), aryl boronic acid (1.5 mmol), potassium phosphate (3 mmol), potassium bromide (2.4 mmol) and tetrakis(triphenylphosphine)palladium (0.05 mmol) in dioxane (10 mL) was heated at reflux overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water and was extracted with ethyl acetate. The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-2: Coupling of Boronic Acid With Triflate

A mixture of triflate (1 mmol), aryl boronic acid (2 mmol), sodium hydrogen carbonate (3 mmol) and tetrakis(triphenylphosphine)palladium (0.05 mmol) or bis(triphenylphosphine)palladium(II)chloride (0.05 mmol) in DME/water (9:1, 10 mL) was heated at reflux overnight. The reaction mixture was cooled, quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-3: Coupling of Tributyltin Derivative With Triflate

A mixture of triflate (1 mmol), tributyltin derivative (3 mmol), tetraethylammonium chloride (6 mmol), and bis(triphenylphosphine)palladium(II)chloride (0.05 mmol) in DMF (10 mL) was heated at 70° C. overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water (20 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-4: Coupling of Trimethyltin Derivative With Triflate

A mixture of triflate (1 mmol), trimethyltin derivative (3 mmol), and bis(triphenylphosphine)palladium(II)chloride (0.05 mmol) in THF (10 mL) was heated at 70° C. overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water and extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-5: Coupling of Alkyne With Triflate

A mixture of triflate (1 mmol), triethylamine (4.5 mmol), substituted alkyne (3.5 mmol), and bis(triphenylphosphine)palladium(II)chloride (0.05 mmol) in DMF (10 mL) was heated at 70° C. overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water (20 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-6: Coupling of Boronate Ester With Aryl Bromides

A mixture of boronate ester (2 mmol), aryl bromide (1 mmol), potassium phosphate (3 mmol) and bis(diphenylphosphinoferrocene)palladium(II)chloride (0.05 mmol) in DMF (10 mL) was heated at 100° C. for overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water (20 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the desired product.

D-7: Coupling of Boronate Ester With Aryl Bromides

A mixture of boronate ester (2 mmol), aryl bromide (1 mmol), sodium hydrogen carbonate (3 mmol) and bis(diphenylphosphinoferrocene)palladium(II)chloride (0.05 mmol) in DME/water (9:1, 10 mL) was heated at 50-70° C. for overnight under an argon atmosphere. The reaction mixture was cooled, quenched with water (20 mL) and was extracted with ethyl acetate (2×10 mL). The organic layers were combined, dried and concentrated in vacuo. Purification by flash column chromatography or crystallization gave the coupled product.

D-8: Coupling of Phenol With Boronic Acid

A mixture of phenol (1 mmol), aryl boronic acid (3 mmol), molecular sieves (4A°), pyridine (5 mmol), copper(II)acetate (1 mmol) and bis(triphenylphosphine)palladium(II)chloride (0.05 mmol) in dichloromethane (10 mL) was stirred at room temperature overnight under an argon atmosphere. The reaction mixture was cooled, filtered through a pad of Celite and concentrated in vacuo. Purification of the crude by flash column chromatography gave the coupled aryl ether.

D-9: Coupling of Trimethyltin Derivative With Triflate

To a solution of triflate (1 mmol), LiCl (4 mmol), PPh₃ (0.15 mmol), CuBr (0.2 mmol), and bis(triphenylphosphine)palladium(II)chloride (0.07 g) in DMF (10 mL) under an atmosphere of argon was added trimethylstannyl compound (0.8 mmol) and a crystal of 2,6-di-t-butyl-4-methylphenol. After the mixture was stirred at 90° C. for 3 h, a second portion of aryi-trimethylstannyl compound (0.5 mmol) was added. The reaction mixture was stirred at 90° C. overnight. Water was added and extracted with ethyl acetate. The organic layer was dried (MgSO₄), concentrated and purified by flash column chromatography or crystallization to furnish the desired coupled product.

D-10: Coupling of Amine With Triflate

A mixture of triflate (0.75 mmol), amine (0.9 mmol), potassium phosphate (1.1 mmol), 2-(di-t-butylphosphino)biphenyl (0.015 mmol) and tris(dibenzylideneacetone)dipalladium(0) (10 mg) in DME (10 mL) was heated at reflux overnight under an argon atmosphere. The reaction mixture was concentrated in vacuo and the residue was purified by flash column chromatography to furnish the desired coupled product.

D-11: Conversion of Triflate to Cyano Compound

To a solution of triflate (0.84 mmol), zinc cyanide (0.54 mmol), Palladium acetate (0.016 mmol), 2-(di-tert-butylphosphine)biphenyl (0.016 mmol) and N-methyl pyrrolidine (10 mL) was heated under argon at 160° C. for 48 h. The reaction mixture was cooled to room temperature and quenched with water (50 mL). The reaction mixture was extracted with ethyl acetate (2×25 mL). The organic layers were combined, dried, filtered and concentrated in vacuo. The residue obtained was purified by flash column chromatography to furnish the desired cyano compound.

D-12: Coupling of Tetravinyltin With Triflate or Halide

To a solution of aryl triflate or bromide (1 mmol) in DMF (5 mL) were added LiCl (5 mmol), tetravinyltin (2 mol), and dichlorbis(triphenylphosphine)palladium (II) (0.01 mmol). The reaction mixture was stirred at 70° C. under nitrogen for 5 h and then diluted with ethyl acetate and filtered. The organic layer was washed with water and brine and dried (MgSO₄). After evaporating the solvent in vacuo, the compound was purified by flash-column chromatography to give the desired product.

E: Oxidation of Aryl Aldehyde to Acid

A mixture of aldehyde (1 mmol), tert-butanol (5 mL), water (2 mL) and acetonitrile (1 mL, additional amount may be added until the reaction mixture was homogenous) was stirred at room temperature. The solution was cooled in ice-bath and 2-methyl-2-butene (1 mL), sodium chlorite (6 mmol) and sodium dihydrogenphosphate (1.6 mmol) were added. The reaction mixture was stirred at room temperature for 2 h. If the solid separated out, the mixture was filtered to collect the solid, the desired product. If no solid separated out, then the reaction mixture was concentrated in vacuo to remove acetonitrile, diluted with water (10 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined, washed with water, brine, dried and concentrated in vacuo to furnish crude acid. Purification was achieved, if needed, by crystallization or using flash column chromatography to obtain pure acid.

E-2: Oxidation of Vinyl Compound to Acid

To a solution of vinyl compound (1 mmol) in acetone (5 mL) was added KMnO₄ (4 mmol). The reaction mixture was stirred for 3 h (the reaction is exothermic, and refluxed on its own during the addition of KMnO₄). The reaction mixture was diluted with methanol and water and filtered. The organic solvents were evaporated in vacuo and the aqueous layer was acidified to pH 1 and extracted several times with ethyl acetate/DME. The combined organic layers were dried (MgSO₄) to furnish the desired acid.

F: Conversion of Aromatic Acid to MEM Ester

To a solution of aromatic acid (1 mmol) in THF (10 mL) was added diisopropylethylamine (2 mmol) and 2-methoxyethoxymethylchloride (1.1 mmol). The reaction mixture was stirred a room temperature for 3 h and diluted with ether (25 mL). The reaction mixture was washed with water (10 mL), brine (10 mL), dried and concentrated in vacuo to obtain product as colorless oil. The product was purified by flash column chromatography to furnish desired product.

G: Conversion of Aromatic Benzyl Ether to Aromatic Phenol, Benzyl Ester to Acid, Benzyl Carbamate to Amine, Alkene to Alkane, Azide to Amine, Nitro to Amine, and Oxime to Amine

To a solution of appropriate substrate (1 mmol) in ethanol (10 mL) was added 10% palladium on carbon (10-wt %). The reaction mixture was hydrogenated at 50 psi for 2 to 24 h (until all starting material disappeared as confirmed by MS and TLC analysis). The catalyst was removed by filtration through a pad of Celite under nitrogen. The filtrate was concentrated in vacuo to furnish the product, which was purified by flash column chromatography or crystallization.

H: Conversion of Aromatic Acid to Benzyl Ester

To a solution of aromatic acid (1 mmol) in DMF (10 mL) was added sodium bicarbonate (1.05 mmol), and benzyl bromide (1.05 mmol) and stirred at room temperature for 24 h. The reaction mixture was quenched with ice water and extracted twice with ethyl acetate. The organic layers were combined, washed with water and brine, dried and concentrated in vacuo to furnish crude product. Purification by crystallization or flash column chromatography gave the desired ester.

I-1: Hydrolysis of MEM Ester to Acid

To a solution of MEM ester (1 mmol) in DME (8 mL) was added 6 N HCl (2 mL) and stirred at room temperature overnight. The reaction mixture was neutralized with solid sodium hydrogen carbonate (18 mmol) and concentrated in vacuo. The reaction mixture was acidified with 0.5 N HCl (20 mL) and extracted with ethyl acetate (2×20 mL). The organic layers were combined, washed with brine (20 mL), dried and concentrated in vacuo to furnish crude product. Purification of the crude by flash column chromatography gave the product. Alternatively the crude reaction mixture was diluted with water (10 mL) and concentrated in vacuo to remove DME. The solid obtained was collected by filtration and dried in vacuo to furnish pure acid.

I-2: Hydrolysis of Ester to Acid

To a solution of ester (1 mmol) in MeOH (10 mL) was added 1 N NaOH (10 mmol). The reaction mixture was stirred at room temperature for 2-3 h, filtered through a plug of cotton, and concentrated in vacuo to remove MeOH. The pH of the aqueous layer was adjusted to below 7. The solid that separated, was collected by filtration, washed with water and dried in vacuo to furnish the desired acid.

J: Coupling of Acid With Amino Compounds

To a solution of acid (1 mmol) in DMF (5 mL) was added corresponding amine (1.1 mmol) and stirred at room temperature until homogenous. Pyridine (5 mL) was added to the reaction mixture followed by 1,3-dicyclohexylcarbodiimide (1.2 mmol) and stirred overnight at room temperature. The mixture was quenched with 6 N HCl (10 mL), diluted with ice cold water (10 mL) and extracted with chloroform (2×10 mL). The organic layers were combined washed with brine (10 mL), dried and filtered. Purification of the crude by flash column chromatography gave the product as a solid. If the product was soluble in water, then the reaction mixture was concentrated in vacuo to remove pyridine and DMF and purified by flash column chromatography.

K: Reduction of Aldehyde to Alcohol

To a solution of aldehyde (1 mmol) in THF (10 mL) was added sodium borohydride (0.4 mmol). The reaction mixture was stirred for 30 mins and quenched with glacial acetic acid (0.3 mL). The reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined and washed with brine (10 mL), dried, filtered and concentrated in vacuo to obtain crude product which was purified by flash column chromatography.

L: Conversion of Vinyl Group to Diol

To a solution of vinyl compound (1 mmol) in THF/tert-butanol (1:1, 10 mL) and water (2 mL) was added 4-methylmorpholine N-oxide (2.5 mmol) and osmium tetraoxide (1 mL, 2.5 wt % in tert-butanol, 0.1 mmol). The reaction mixture was stirred at room temperature for 2 h and quenched with saturated aqueous solution of sodium sulfite (5 mL). The reaction was stirred at room temperature for 30 mins and diluted with brine (10 mL) and ethyl acetate (10 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (10 mL). The organic layers were combined and washed with brine (10 mL), dried, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography to furnish the desired diol.

M: Conversion of Diol to Aldehyde

To a solution of diol (1 mmol) in DME/water (9:1, 10 mL) was added sodium metaperiodate (3 mmol) and stirred at room temperature for 30 min. The reaction mixture was quenched with water (10 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined and washed with brine (10 mL), dried, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography to furnish the desired aldehyde.

N: Conversion of Alcohol to Mesylate

To a solution of alcohol (1 mmol) in DME (10 mL) was added dimethylaminopyridine (0.1 mmol), methane sulfonyl chloride (3 mmol) and diisopropylethylamine or triethylamine (5 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (2×10 mL). The combined organic layers were washed with brine, dried, filtered and concentrated in vacuo. The residue obtained, was purified by column chromatography to furnish the desired mesylate.

O: Conversion of Mesylate to Azide

To a solution of mesylate (1 mmol) in DMSO (10 mL) was added sodium azide (25 mmol) and heated at 100° C. overnight. The reaction mixture was cooled and diluted with cold water (25 mL). The reaction mixture was extracted with ethyl acetate (2×15 mL). The combined organic layers were washed with water (10 mL), brine (10 mL), dried, filtered and concentrated in vacuo The residue obtained was purified by column chromatography to furnish the desired azido compound.

P: Protection of Amine as Benzyl Carbamate

A mixture of amino compound (1 mmol), benzyl chloroformate (2 mmol) and triethylamine (10 mL) in pyridine (10 mL) was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo to remove organic solvents and diluted with 0.1 N HCl (10 mL). The product was extracted with chloroform (2×10 mL), dried, filtered and concentrated in vacuo. The residue obtained was purified by column chromatography to furnish the desired carbamate.

Q: Conversion of Silyl Protected Amine to Amine

A mixture of silyl protected amine (1 mmol), tetrabutylammonium fluoride (1.0 M in THF, 2 mmol) in THF (10 mL) was stirred at room temperature for 1.5 h. The reaction mixture was concentrated in vacuo and purified by column chromatography to obtain the desired product.

R: Protection of Amine as tert-Butyl Carbamate

To a solution of amino compound (1 mmol) in acetonitrile (5 mL) was added triethylamine (2 mmol) and BOC anhydride (1.2 mmol). The reaction mixture was stirred for 2 h and concentrated in vacuo. Water was added to the residue and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO₄), and the solvent was evaporated in vacuo to furnish tert-butyl carbamate. If needed, the product was purified by crystallization or column chromatography.

S: Conversion of tert-Butyl Carbamate to Amine

To a solution of tert-butyl carbamate (1 mmol) in dichloromethane (10 mL) was added trifluoroacetic acid (2 mL). The solution was stirred at room temperature for 4 h and concentrated in vacuo. The residue was purified by column chromatography or crystallization to give the desired amine.

S-2: Conversion of tert-Butyl Carbamate to Amine

To a solution of tert-butyl carbamate (1 mmol) in methanol (13 mL) was added 6 N HCl (8.75 mL, 52 mmol) and water (4.25 mL). The reaction mixture was stirred at room temperature for 2 days. The pH was adjusted to 7 using conc. ammonium hydroxide and the solid that separated out, was collected by filtration, washed with ether, dried in vacuo to furnish the desired product. If no solid separated out, the product was isolated by extraction with chloroform and evaporating the organic layer.

T: Protection of Aldehyde as Acetal

To a solution of aldehyde (1 mmol) in ethanol (5 mL) was added triethyl orthoformate (1.4 mmol), ammonium nitrate (0.2 mmol) and stirred at room temperature overnight (if reaction was not complete by TLC and NMR analysis of an aliquot, the reaction mixture was heated at 50° C. until complete). After completion of the reaction, the mixture was quenched with triethylamine (0.2 mmol) and concentrated in vacuo to remove ethanol. The residue was dissolved in ether, filtered to remove any insoluble inorganic impurities, and evaporated to dryness. The product obtained was used as such without further purification.

U-1: Conversion of Bromide to Boronic Acid

To a mixture of bromo compound (1 mmol) in ether (10 mL), cooled to −78° C., n-butyl lithium (1.2 mmol) was added dropwise and the reaction mixture was stirred for 30 mins after the addition was completed. Tributyl borate (1.3 mmol) in ether (10 mL) was added to the reaction and stirred at −78° C. for 2 h. The reaction mixture was allowed to warm to 0° C. and quenched with 2 M HCl (10 mL). The reaction mixture was stirred at room temperature for 1 h and cooled with ice. The aqueous layer was separated and the organic layer was extracted twice with 1N NaOH (2×10 mL). The basic extracts were combined and washed with ether (10 mL). The basic layer was acidified to pH 4 using 6 N HCl and the solid that separated out was collected by filtration, washed with water and hexane and dried in vacuo to furnish boronic acid as a solid. If no solid product is obtained then the basic layer was extracted with ether (2×10 mL). The organic layers were combined, dried and concentrated in vacuo to furnish boronic acid.

U-2: Synthesis of Boronic Acid by Ortho Lithiation of Aryl Aldehyde

To a solution of N,N,N′-trimethylethylenediamine (1 mmol) in THF/ether (10 mL, 1:1) cooled to −20° C. was added dropwise, over a period of 15 mins, n-butyl lithium (1 mmol) and stirred at −20° C. for 15 mins. Aldehyde (1 mmol) at −20° C. was added dropwise over a period of 10 mins to this mixture. The reaction mixture was further stirred for 15 mins at −20° C. followed by the addition of n-butyl lithium (2.8 mmol) dropwise over a period of 15 mins and stirred at 4° C. overnight. The reaction mixture was cooled to −40° C. and tributyl borate (5.6 mmol) in ether (20 mL) was added to the reaction and stirred at 4° C. for 12 h. The reaction mixture was allowed to warm to 0° C. and quenched with 2 M HCl (3 mmol) and heated at reflux for 2 h and added to ice water (25 mL). The aqueous layer was separated and the organic layer extracted twice with 1N NaOH (2×10 mL). The basic extracts were combined and washed with ether (10 mL). The basic layer was acidified to pH 3 using 6 N HCl and the solid that separated out was collected by filtration, washed with water and hexane and dried in vacuo to furnish boronic acid as a solid. If no solid product was obtained, then the basic layer was extracted with ether (2×10 mL). The organic layers were combined, dried and concentrated in vacuo to furnish boronic acid.

U-3: Synthesis of Boronic Acid by Ortho Lithiation of Aryl Acetal

To a solution of aryl acetal compound (1 mmol) in ether (10 mL) at −78° C., tert-butyl lithium (1.1 mmol) was added dropwise and the reaction mixture was stirred for 3 h at −20° C. after the addition was completed. Tributyl borate (1.2 mmol) in ether (10 mL) was added to the reaction and stirred at −20° C. for 1 h. The reaction mixture was allowed to warm to 0° C. and quenched with 2 M HCl (10 mL). The reaction mixture was stirred at room temperature for 1 h. The aqueous layer was separated and the organic layer was extracted twice with 1N NaOH (2×10 mL). The basic extracts were combined and washed with ether (10 mL). The basic layer was acidified to pH 4 using 6 N HCl and the solid that separated out was collected by filtration, washed with water and hexane and dried in vacuo to furnish boronic acid as a solid. If no solid product was obtained then the mixture was extracted with ether (2×10 mL). The organic layers were combined, dried and concentrated in vacuo to furnish boronic acid.

V-1: Demethylation of Aryl Methyl Ether to Phenol

In a round bottom flask (50 mL), pyridine hydrochloride (10 g) was heated in an oil bath at 180° C. After the entire solid had melted, the corresponding aryl methyl ether (1 mmol) was added in small portions over a period of 20 min. The reaction mixture was heated at 180° C. for 4 h, cooled and quenched with water (100 mL). The reaction mixture was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine, dried over MgSO₄, concentrated to give phenol. This can be further purified if needed by crystallization or column chromatography.

V-2: Demethylation of Aryl Methyl Ether to Phenol

To a solution of aryl ether (1 mmol) in dichloromethane (10 mL) cooled to −78° C. was added boron tribromide (3 mmol). The reaction mixture was allowed to warm to room temperature overnight and quenched with water (10 mL). The solid obtained was collected by filtration to give the desired product. More product was obtained after evaporation of the organic layer and washing the residue with water. Alternatively, if a homogenous biphasic mixture was obtained on addition of water, the organic layer was separated, washed with brine, dried over MgSO₄, and concentrated to give the desired phenol. This can be further purified if needed by crystallization or column chromatography.

V-3: Demethylation of Aryl Methyl Ether to Phenol

To a solution of aryl methyl ether (1 mmol) in dichloromethane (5 mL) was added AlCl₃ (8.5 mmol). The reaction mixture was heated to reflux for 12 h under nitrogen. To this mixture was added 12 mL of 1 N HCl slowly and the organic layer was separated. The aqueous layer was re-extracted several times with ethyl acetate/DME. The combined organic layers were washed with brine, dried (MgSO₄), and evaporated in vacuo to furnish the desired phenol, which was purified by column chromatography.

V-4: Demethylation of Aryl Methyl Ether to Phenol

To a stirred slurry of NaH (2 mmol) in anhydrous toluene (5 mL) under nitrogen atmosphere was added para-thiocresol (2 mmol) dissolved in toluene (40 mL). The mixture was stirred at room temperature for 30 min and hexamethylphosphoric triamide (2 mmol) in toluene (5 mL) was added dropwise over a period of 30 min. A solution of aryl ether (1 mmol) in toluene (5 mL) was added in one portion. The reaction mixture was stirred at reflux for 9.5 h, cooled to room temperature and diluted with ethyl acetate (40 mL). The organic layer was extracted with 1 N aqueous NaOH solution (2×20 mL). The basic layer was acidified to pH 5 and extracted with ethyl acetate (2×20 mL). The organic layers were combined, washed with water, dried (MgSO₄) and concentrated in vacuo. The residue obtained was purified by flash column chromatography to afford the desired phenol compound.

W: Conversion of Acid to Methyl Ester

A mixture of acid (1 mmol), conc. H₂SO₄ or conc HCl (0.5 mL) and methanol (10 mL) was heated at reflux for 16 h. The mixture was concentrated to half of its volume and the residue poured into a saturated sodium bicarbonate solution. The precipitate was collected by filtration, washed with water and dried to give the desired ester. If the ester did not come as solid, it was extracted with ethyl acetate. The organic layer was dried, filtered and concentrated to give the desired ester.

W-2: Conversion of Acid to Ester

A solution of methanolic HCl or ethanolic HCl was prepared by the addition of acetyl chloride (1 mL) to methanol/ethanol (9 mL) at 0° C. and stirred for 30 mins. To the solution of anhydrous methanolic HCl was added acid (1 mmol) and stirred at room temperature (or reflux if needed) overnight. The reaction mixture was concentrated to dryness in vacuo and the residue was purified by column chromatography or crystallization to furnish the desired ester.

X: Conversion of Phenol to Alkyl Aryl Ethers or Alkylation of Amines

To a solution phenol or amine (1 mmol) in DMF (10 mL) was added cesium carbonate (1.25 mmol) and corresponding bromide (1.1 mmol). The reaction mixture was stirred at room temperature overnight and quenched with water (25 mL). The product was extracted with ether (2×25 mL), the organic layers were combined and washed with water (25 mL), brine (25 mL), dried and concentrated in vacuo to furnish crude product. The crude was purified by crystallization or flash column chromatography.

Y: Conversion of Nitrile to Hydroxycarbamimidoyl

To a solution of nitrile compound (1 mmol) in ethyl alcohol (10 mL) was added hydroxylamine (50% aqueous solution, 5 mmol). The mixture was stirred at reflux for 2-5 h. The reaction mixture was concentrated in vacuo to furnish the desired hydroxycarbamimidoyl compound.

Z: Opening of Aromatic Methylene Dioxy Compound With Alcohol

A solution of potassium tert-butoxide (2.25 mmol) in DMSO (1.25 mL) was heated at 50° C. for 30 min. Methanol (1.25 mL) was added to it and continued heating at 50° C. for 30 min. To the reaction mixture was added 1,2-methylenedioxy aromatic compound (1 mmol) and continued heating at 50° C. for 30 min. The reaction mixture was cooled to room temperature and quenched with water (10 mL) and 1 N sodium hydroxide (16 mL). The reaction m mixture was washed with ether (2×10 mL) and acidified to pH 4 using conc HCl. The solid obtained was collected by filtration to furnish the desired product.

Z-1: Opening of Aromatic Methylene Dioxy Compound With Alcohol

To a mixture of methylene dioxy compound (1 mmol) in HMPA (2.5 mL) were added sodium methoxide (2.5 mmol) and heated with stirring at 150° C. for 12 min. The mixture was cooled and poured into ice water (20 mL), NaOH (30 mg) and stirred for 10 min. It was then extracted with ether and the aqueous layer was acidified to pH 4 with HCl and extracted with ether. The later ethereal extracts were combined, dried and concentrated. The residue was purified by crystallization or column chromatography.

AA: Conversion of Amine to Amide in the Presence of a Phenol

To a solution of amino compound (1 mmol) in pyridine (5 mL) was added, dropwise, acid chloride (2 mmol) at 0° C. under N₂. The mixture was stirred for 45 min and was then poured into ice water and acidified with 1 N HCl. The precipitated solid was collected by filtration, washed with 1N HCl, hexane, and then dried in vacuo to give crude product. The crude product was added to freshly prepared sodium methoxide solution (0.1 M, 10 mL) and stirred for 30 min at room temperature. The reaction mixture was quenched with acetic acid (1 mmol) and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water. The water layer was extracted with ethyl acetate, and the combined organic layers were washed with brine, dried (MgSO₄) and evaporated to yield a solid. The solid was washed with hexane and dried in vacuo to furnish the desired amide.

AB-1: Conversion of Amino of Amidine to Amino Carbamate

To amidine compound (1 mmol) was added 0.1N NaOH (10 mL) and stirred at room temperature for 5 min. The reaction mixture was concentrated in vacuo and to the residue was added alkyl or aryl 4-nitrophenyl carbonate (2 mmol) in 20 mL of hexamethylphosphoramide and stirred at 45° C. for 24 h. The reaction was quenched with water (100 mL) and extracted with ethyl acetate (2×100 mL). The combined extracts were washed with water (100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue obtained was purified by flash column chromatography to furnish the desired product.

AB-2: Conversion of Amino of Amidine to Amino Carbamate

To a solution of amidine compound (1 mmol) in acetonitrile (25 mL) was added triethylamine (5 mL) and aryl/alkyl chloroformate (2 mmol) or dialkyl/aryl carbonate. The reaction mixture was stirred at room temperature for 16 h and quenched with water (100 mL). The reaction mixture was extracted with ethyl acetate (2×100 mL). The combined extracts were washed with brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue obtained was purified by flash column chromatography to furnish the desired product.

AC: Conversion of Aldehyde to Oxime

To a stirred solution of aldehyde (1 mmol) in ethanol (10 mL) was added pyridine (10 mL) and hydroxylamine hydrochloride (1.25 mmol). The reaction mixture was stirred overnight at room temperature under nitrogen and then concentrated in vacuo to one third of its original volume. Water (10 mL) was added and the precipitated solid was collected by filtration and dried in vacuo. The product was used as such for next step without further purification.

AD: Debenzylation in the Presence of Aldehyde

To a solution of phenyl methoxyaryl aldehyde (1 mmol) in dichloromethane (10 mL) cooled to −78° C. was added dropwise under a nitrogen atmosphere boron tribromide (1M solution in dichloromethane, 1.2 mmol). The reaction mixture was allowed to warm to room temperature and stirred at room temperature overnight. The reaction mixture was quenched with water (10 mL) and the layers were separated. The aqueous layer was extracted with chloroform (10 mL). The organic layers were combined, washed with brine (10 mL), dried, filtered and concentrated in vacuo to furnish crude product. Purification of the crude by flash column chromatography furnished the desired phenolic aldehyde

AE-1: Reductive Amination of Aldehyde

To a stirred solution of aldehyde (1 mmol) in methanol (40 mL) was added amine (3.3 mmol) followed by the addition of glacial acetic acid (0.3 mL). The reaction mixture was stirred for 30 min under nitrogen at room temperature, and then sodium cyanoborohydride (1.5 mmol) was added. After stirring for 20 min the solvent was evaporated in vacuo, and the residue was taken in ethyl acetate. The organic layer was washed with water, and the insoluble material was removed from the organic layer by filtration. The pH of the aqueous phase was adjusted to 7 with 1N NaOH and was extracted twice with ethyl acetate. The combined organic layers were washed with brine and dried (MgSO₄). The solvent was evaporated in vacuo to furnish crude product. The crude product was purified by crystallization or flash column chromatography.

AE-2: Reductive Amination of Aldehyde

To a mixture of aminoarylamidine (1.2 mmol), 4A° molecular sieves, and sodium hydroxide (1 N solution in anhydrous methanol, 1.2 mL, 1.2 mmol) in methanol (10 mL) was added a solution of aldehyde (1 mmol) in THF (10 mL). The reaction mixture was heated for 15 mins at reflux temperature and was cooled to room temperature. Acetic acid (1%) and sodium cyanoborohydride (1 M solution in THF, 5 mmol) was added to the reaction mixture and stirred at room temperature overnight. The reaction mixture was quenched with 1 N NaOH (30 mmol) and stirred for additional 2 h and concentrated in vacuo to remove methanol. The mixture was diluted with water (15 mL) and washed with ether (2×10 mL). The aqueous layer was acidified to pH 2 using 6 N HCl and the solid that separated out was collected by filtration, washed with ether, dried in vacuo to furnish product, which was purified by flash column chromatography, if needed.

AE-3: Reductive Amination of Aldehyde

A mixture of aminoarylamidine (2 mmol), 4A° molecular sieves, pyridine (6 mL) in methanol (9 mL) was heated at 50° C. for one hour. A solution of aldehyde (1 mmol) in methanol (7.5 mL) containing acetic acid (1%) was added and continued heating for 4 h to 12 h. The reaction mixture was cooled and sodium cyanoborohydride (1 M solution in THF, 5 mmol) was added to the reaction mixture and stirred at room temperature overnight. The reaction mixture was quenched with 5 N NaOH (30 mmol) and stirred for additional 2 h. The reaction mixture was filtered through Celite (to remove molecular sieves) and concentrated to remove methanol. The mixture was diluted with water (15 mL) and washed with ether (2×10 mL). The aqueous layer was filtered and solid obtained was kept aside (mainly product). The aqueous layer was acidified to pH 2 using 6 N HCl and the solid that separated out was collected by filtration. The combined solid materials were purified, if needed, by flash column chromatography.

AE-4: Reductive Amination of Aldehyde

To a mixture of aldehyde (1 mmol) and aminoarylamidine (1.1 mmol) in MeOH at room temperature was added triethyl amine (2.75 mmol), sodium cyanoborohydride (0.83 mmol) and zinc chloride (0.9 mmol). The reaction mixture was stirred at room temperature overnight and concentrated to remove methanol. The reaction mixture was quenched with 1 N NaOH (10 mL), diluted with water (10 mL), and extracted with EtOAc (5×20 mL). The combined organic extracts were washed with brine (15 mL), dried (MgSO4), filtered through Celite and concentrated to give the product. Purification of the crude by flash column chromatography gave the desired product.

AE-5: Reductive Amination of Aldehyde

To a solution of amine (1.2 mmol) in MeOH (10 mL) was added aldehyde (1 mmol) in THF (10 mL) containing acetic acid (0.1 mL) drop-wise. The mixture was stirred at 50° C. for 4-12 h and then cooled to room temperature. Sodium cyanoborohydride (1.5 mmol) was added to the reaction mixture and stirred at room temperature overnight. Water was added and pH of the solution was adjusted to 7. The solution was extracted with ethyl acetate. The organic layer was dried (MgSO₄) and evaporated in vacuo. The residue was purifeid by flash column chromatography to furnish the desired amine.

AF-1: Synthesis of Amidine From Nitrile

Acetyl chloride (5 mL) was added to methanol (5 mL) at 0° C. drop-wise and stirred at room temperature for 15 mins. To this solution of methanolic HCl was added nitrile compound (1 mmol) and stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and dried. The residue obtained of the resulting methyl imidate was dissolved in methanol (10 mL). Dry ammonia gas was bubbled into the reaction mixture at reflux temperature for 5 h. The reaction mixture was concentrated to furnish the required amidine.

AG: Addition of Grignard Reagent to Aryl Aldehyde

To a solution of aryl aldehyde (1 mmol) in THF (15 mL) cooled to −78° C. was added drop wise under a nitrogen atmosphere, vinyl magnesium bromide (1 M solution in THF, 5 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 48 h. The reaction was quenched carefully with saturated aqueous ammonium chloride solution (10 mL) and extracted with ethyl acetate (2×10 mL). The organic layers were combined, washed with brine (10 mL), dried and concentrated in vacuo. The residue obtained was purified by flash column chromatography to obtain the desired addition product.

AG-1: Synthesis of Tributylvinyltin Compounds From Vinyl Bromide Containing Hydroxyl

To a solution of vinyl bromide with hydroxyl (1 mmol) in dichloromethane (20 mL) was added tert-butyldimethylsilyl chloride (1.5 mmol) and DMAP (1.5 mmol) and stirred at room temperature overnight. The reaction mixture was quenched with water (20 mL) and the aqueous layer separated. The organic layer was washed with 0.1 N aqueous HCl (10 mL), brine (20 mL), dried and concentrated in vacuo to furnish corresponding tert-butyldimethylsilyloxy compound as an oil which was used as such for the next step.

To a solution of the above oily residue (1 mmol) in diethyl ether (20 mL) cooled to −78° C. was added dropwise tert-butyllithium (1.7 M in pentane, 2 mmol) over a period of 15 mins. The reaction mixture was stirred at −78° C. for 3 h and quenched at −78° C. with 2 N aqueous sulfuric acid (2 mL) and water (18 mL). The reaction mixture was neutralized using 2 N NaOH and the organic layer was separated. The organic layer was washed with water (20 mL), brine (20 mL), dried and concentrated in vacuo. Purification of the crude residue obtained by flash column chromatography furnished the desired tributyltin compound.

AG-2: Synthesis of Tributylmethyltin Compounds From Arylmethyl Bromides or Allyl Bromides

To lithium clippings (10 mmol) in THF (10 mL) cooled to −40° C. was added dropwise tributyltin chloride (0.27 mL, 1 mmol) in THF (5 mL) over a period of 15 min. The reaction mixture was allowed to warn to room temperature and stirred for 16 h. The reaction mixture was filtered through glass wool to remove insoluble impurities and cooled to −40° C. A freshly prepared solution of arylmethyl bromide or allyl bromide (1 mmol) was added dropwise over a period of 10 mins and stirred at room temperature overnight. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (10 mL) and extracted with ether (2×10 mL). The organic layers were combined, washed with brine (10 mL), dried, filtered and concentrated in vacuo to furnish desired tributyltinalkyl and was used as such without further purification.

AG-3: 4-Bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic Acid Methyl Ester

To a mixture of 2-bromo-3,4-dihydroxy-benzaldehyde (2.17 g, 10.0 mmol) and K₂CO₃ (5.56 g, 40.2 mmol) in n-propanol (25 mL) was added dibromoacetic acid (2.18, 10.0 mmol) and the mixture was heated at reflux temperature for 24 h. After cooling to room temperature, another portion of dibromoacetic acid (1.75 g, 8.0 mmol) was added. The mixture was stirred at reflux for 46 h. n-Propanol was evaporated and water (30 mL) was added. The resulting aqueous solution was acidified to pH 2 by adding 1 N HCl and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried (MgSO₄) and evaporated in vacuo to afford crude 4-bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid (1.34 g) as a brownish solid. This crude product was dissolved in anhydrous methanol (50 mL) and conc. H₂SO₄ (5 mL) was added drop by drop. The resulting mixture was refluxed overnight and cooled to room temperature. Water (50 mL) was added and the resulting aqueous solution was extracted with ethyl acetate (100 mL×3). The combined organic layers were dried (MgSO₄) and evaporated in vacuo. The residue was purified by flash column chromatography (ethyl acetate:hexane=5:95) to furnish 4-bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid methyl ester as a white solid.

AH: Synthesis of tert-Butyl Ester of Phenol

To a solution of phenol (1 mmol) in pyridine (10 mL) was added 2,2-dimethylpropionyl chloride (1.2 mmol) dropwise. The mixture was stirred at room temperature for overnight and diluted with water (100 mL). The reaction mixture was extracted with ethyl acetate (3×50 mL). The organic layers were combined and washed with aqueous 0.5 N HCl (100 mL), water, brine, dried (MgSO₄) and concentrated in vacuo. The crude residue was purified by flash column chromatography to furnish the desired ester.

AI: Preparation of 2-Bromo-5-hydroxy benzaldehyde

To a solution 3-hydroxybenzaldehyde (Aldrich, 101.39 g, 805 mmol) in chloroform (1000 mL), was added bromine (45 mL, 845 mmol) in chloroform (200 mL) drop wise over a period of 2 h at room temperature. The reaction mixture was stirred at room temperature overnight and filtered to collect crude 2-bromo-5-hydroxy benzaldehyde (32 g) as a dark brown solid. The filtrate was concentrated to 200 mL, filtered through a pad of Celite and silica gel (40 g) and washed with ether (1000 mL). The filtrate was concentrated in vacuo to give a second crop of the crude desired aldehyde (60 g) as a dark brown solid. The above solids were combined and dissolved in glacial acetic acid (360 mL) by heating. Water (840 mL) was added and the solution was filtered hot. The solution was allowed to attain room temperature and kept in a refrigerator overnight. The crystals obtained were collected by filtration and washed with water, dried overnight in vacuo to furnish (60 g, 37%) of the desired product as a purplish brown crystalline solid, mp: 135° C.

AJ-1: Amidine From Nitrile

A mixture of nitrile (1 mmol) and hydroxylamine (aqueous 50%, 1.8 mL) in EtOH (15 mL) was refluxed for 3 h and concentrated in vacuo. To the residue obtained was added EtOH (20 mL), acetic acid (2 mL) and a small amount of Raney nickel. The reaction mixture was hydrogenated (50 psi) for 14-24 h, filtered and concentrated in vacuo. The residue obtained, was purified by flash column chromatography to obtain the corresponding amidine.

AJ-2: Amidine From Nitrile

A mixture of nitrile (1 mmol) and saturated methanolic HCl solution (freshly prepared by bubbling HCl gas or prepared in-situ by premixing methanol and acetyl chloride at ice cold temperature) was stirred at room temperature overnight. The reaction mixture concentrated in vacuo to furnish methyl imidate. To the residue of methyl imidate was added MeOH (40 mL) and ammonia gas was bubbled at reflux temperature for 16 h or till the reaction was complete. The reaction mixture was concentrated in vacuo and dried to furnish the desired amidine. Alternatively, the methyl imidate was dissolved in methanol and ammonium acetate (10 mmol) was added. The reaction mixture was concentrated in vacuo and purified by flash column chromatography to obtain the corresponding amidine.

AJ-3: Amidine From Nitrile

To a solution of nitrile (1 mmol) dissolved in methanol (5 mL) was added N-acetyl cystein (0.1 or 1 mmol) and ammonium acetate (5 mmol) and heated at reflux till the reaction was complete. The reaction mixture was concentrated in vacuo and purified by flash column chromatography to obtain the corresponding amidine.

AK: Conversion of Aryl Triflates or Halides to Boronate Ester

To dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.75 mmol) under argon in dioxane (100 mL) was added aryl triflate (25 mmol), pinacolborane (31.5 mmol) and triethylamine (75 mmol). The reaction mixture was heated under argon at 100° C. for 3 h or until complete as evidenced from TLC analysis. The reaction mixture was concentrated in vacuo. The residue obtained was purified by flash column chromatography to furnish the desired boronate ester. Alternatively, the following method can be used.

To dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (0.03 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.03 mmol) under argon in dioxane (100 mL) was added aryl triflate (1 mmol), bis(pinacolata)diboron (1.1 mmol) and potassium acetate (3 mmol). The reaction mixture was heated under argon at 100° C. for 3 h or until complete as evidenced from TLC analysis. The reaction mixture was concentrated in vacuo. The residue obtained was purified by flash column chromatography to furnish the desired boronate ester.

The examples of the compounds prepared are given in the following tables. The tables describe the compounds, their method of preparation, the starting material, and the analytical data. In some cases, where analytical data have not been given, those compounds were characterized at the later step in the synthesis.

AL: Deprotection of the Benzyl Ester

The aldehyde (1 mmol) was mixed with ammonium nitrate (0.2 mmol) in 10 mL of EtOH. The mixture was treated with HC(OEt)₃ (1.5 mmol) and stirred at 70° C. for 2 h. The reaction mixture was diluted with 30 mL of EtOH and dried with molecular sieves followed by filtration.

The above filtrate (40 mL) was treated with 1 drop of concentrated HCl and 10% Pd/C (0.1 g) followed by hydrogenation for 5 h. The reaction mixture was filtered and concentrated. The residue was treated with 10 mL of DME and 1 mL of 1N HCl followed by stirring at room temperature for 0.5 h. Water (5 mL) was added and the mixture was extracted with EtOAc (2×10 mL). The combined extracts were washed with water (2×10 mL) and brine (10 mL), dried over MgSO₄, filtered, and concentrated. The residue was purified by flash column chromatography (EtOAc/Hex/MeOH, 1:1:0 to 1:1:0.2) to afford the desired product.

AM: Preparation of α-Amino Esters:

A mixture of methyl 2′-formyl-4-[(isobutylamino)carbonyl]-5′-methoxy-1,1′-biphenyl-2-carboxylate (1 mmol) and 4-aminobenzonitrile (1 mmol) in toluene (5 mL) was heated at reflux for 16 h. The reaction mixture was concentrated and the residue taken in dry methanol (5 mL), cooled in an ice bath and tosylmethyl isocyanide (1.1 mmol) added to it followed by BF₃.ethereate (3.0 mmol) over a period of 5 min. The reaction mixture was stirred for 0.5 h in ice-bath and then at room temperature for 1.5 h. Water (90 μL) was added to the reaction and further stirred for 16 h. The reaction mixture was taken in ethyl acetate (50 mL), washed with water and brine, and dried over MgSO₄. After filtration, the filtrate was concentrated and the residue was purified on silica gel using ethyl acetate:hexane as an eluent to give 0.37 g (67%) of the desired product, 2′-{1-[4-cyanophenyl)amino]-2-methoxy-2-oxoethyl}-4-[(isobutylamino)carbonyl]-5′-methoxy-1,1′-biphenyl-2-carboxylate.

No. Starting Method Cpd. —R —R′ From Used Analytical Data 2a —OH

1 A-1 or A-2 ¹H NMR (DMSO-d₆): δ10.26(s, 1H), 9.84(s, 1H), 8.15(d, J=3.0Hz, 1H), 7.64(dd, J=2.0Hz and 8.9Hz, 1H), 6.94(d, J=8.9Hz, 1H), 3.90(s, 3H), 2.15(d, J=6.9Hz, 2H), 2.06(m, J=6.9Hz, 1H), 0.93(d, J=6.9Hz, 1H), 0.93(d, J=6Hz, 6H); MS(ES⁺): 252.12 2b —OH

1 A-1 or A-2 Characterized in the next step 2c —OH

1 A-1 or A-2 MS(ES⁺): 294.54 2d —OH

1 A-1 or A-2 MS(ES⁺): 288.49 (M + Na)⁺ 2e —OH

1 A-1 or A-2 Characterized in the next step 2f —OH

1 A-1 or A-2 MS(ES⁺): 300.40 (M + Na)⁺ 2g —OH

1 A-1 or A-2 MS(ES⁺): 272.48 (M + Na)⁺; MS(ES⁻): 248.66 2h —OH

1 A-1 or A-2 MS(ES⁺): 286.48 (M + Na)⁺ 2i —OH

1 A-1 or A-2 MS(ES⁺): 224.54 2j —OH

1 A-1 or A-2 Characterized in the next step 3a —OSO₂CF₃

2a B-1 or B-2 MS(ES⁺): 384.37 3b —OSO₂CF₃

2b B-1 or B-2 MS(ES⁺): 370.36 3c —OSO₂CF₃

2c B-1 or B-2 MS(ES⁺): 426.37 3d —OSO₂CF₃

2d B-1 or B-2 Characterized in the next step 3e —OSO₂CF₃

2e B-1 or B-2 ¹H NMR(CDCl₃): δ8.41(d, J=2.3Hz, 1H), 8.10(dd, J=8.5, 2.4Hz, 1H), 7.37(d, J=8.5Hz, 1H), 6.48(broad, 1H), 3.98(s, 3H), 3.46(q, J=7.2Hz, 2H), 1.62(m, 2H), 1.42(m, 2H), 0.96(t, J =7.2Hz, 3H); MS(ES⁺): 384.1 3f —OSO₂CF₃

2f B-1 or B-2 ¹HNMR(CDCl₃): δ8.45(d, J=2.4Hz, 1H), 8.14(dd, J=8.7, 2.4Hz, 1H), 7.42(d, J=8.7Hz, 1H), 6.52(broad, 1H), 4.14(m, 2H), 4.00(s, 3H); MS(ES⁺): 410.2 3g —OSO₂CF₃

2g B-1 or B-2 ¹H NMR(CDCl₃): δ8.42(d, J=2.3Hz, 1H), 8.12(dd, J=8.5, 2.3Hz, 1H), 7.39(d, J=8.7Hz, 1H), 6.31(broad, 1H), 4.00(s, 3H), 3.34(dd, J=7.2, 5.5Hz, 2H), 1.07(m, 1H), 0.59(m, 2H), 0.30(m, 2H); MS(ES⁺): 382.2 3h —OSO₂CF₃

2h B-1 or B-2 MS(ES⁺): 396.36 3i —OSO₂CF₃

2i B-1 or B-2 ¹H NMR(DMSO-d₆): δ8.85(t, J=5.5Hz, 1H), 8.49(d, J=2.3Hz, 1H), 8.23(dd, J=8.7, 2.3Hz, 1H), 7.70(d, J=8.7Hz, 1H), 3.92(s, 3H), 3.31(m, 2H), 1.14(t, J=7.2Hz, 3H); MS(ES⁺): 356.1 3j —OSO₂CF₃

2j B-1 or B-2 ¹H NMR(DMSO-d₆): δ8.81(t, J=6.0Hz, 1H), 8.49(d, J=2.3Hz, 1H), 8.24(dd, J=8.7, 2.4Hz, 1H),7.71(d, J=8.7Hz, 1H), 3.92(s, 3H), 3.15(m, 2H), 1.64(m, 1H), 1.41(m, 1H), 1.12(m, 1H), 0.88(m, 6H); MS(ES⁺): 398.2 5 —OSO₂CF₃ —CO₂MEM 4 B-2 ¹H NMR(DMSO-d₆): δ8.52(d, J=2.0Hz, 1H), 8.32(dd, J=2.0 and 8.9Hz, 1H), 7.72(d, J=7.9Hz, 1H), 5.50(s, 2H), 3.88(s, 3H), 3.78(t, J=4.9Hz, 2H), 3.44(d, J=4.9Hz, 2H), 3.17(s, 3H); MS(ES⁺): 439.1 (M + Na)⁺ 6a

3a AK ¹H NMR(CDCl₃): δ8.29(d, J=1.6Hz, 1H), 7.96(dd, J=7.5 & 1.6Hz, 1H), 7.58(d, J=7.5Hz, 1H), 6.24(bs, 1H), 3.94(s, 3H), 3.30(t, J=6.5Hz, 2H), 1.92(m, 1H), 1.43(s, 12H), 0.99(d, J=6.5Hz, 6H); MS(ES⁺) 362.2 139 —OH

138 AA ¹H NMR(DMSO-d₆): δ10.26(s, 1H), 9.84(s, 1H), 8.15(d, J=3.0Hz, 1H), 7.64(dd, J=2.0Hz and 8.9Hz, 1H), 6.94(d, J=8.9Hz, 1H), 3.90(s, 3H), 2.15(d, J=6.9Hz, 2H), 2.06(m, J=6.9Hz, 1H), 0.93(d, J=6.9Hz, 6H); MS(ES⁺): 252.12 140 —OSO₂CF₃

139 B-2 ¹H NMR(DMSO-d₆): δ10.38(s, 1H), 8.36(d, J= 2.8Hz, 1H), 7.99(dd, J=2.6 and 8.9Hz, 1H), 7.52(d, J=9.0Hz, 1H),3.89(s, 3H),2.23(d, J= 7.0Hz, 2H), 2.09(m, J=6.6Hz, 1H), 0.94(d, J= 6.6Hz, 6H); MS(ES⁺): 384.0 169 —OH

168 AC ¹H NMR(CDCl₃): δ8.08(s, 1H), 8.00(d, J=2.3Hz, 1H), 7.75(dd, J=2.3 and 8.7Hz, 1H), 7.01(d, J=8.7Hz, 1H), 3.97(s, 3H), 3.50(s, 1H); MS(ES⁺): 196.1 170 —OH —CH₂NH₂ 169 G ¹H NMR(DMSO-d₆): δ7.79(d, J=2.0Hz, 1H), 7.51(dd, J=2.3 and 8.5Hz, 1H), 6.95(d, J=8.5Hz, 1H), 7.01(d, J=8.7Hz, 1H), 3.90(s, 3H), 3.72(s, 2H), 3.50(bs, 2H); MS(ES⁺): 182.12 171 —OH

170 AA MS(ES⁻): 250.50; MS(ES⁺): 274.50 (M + Na)⁺ 172 —OSO₂CF₃

171 B-2 ¹H NMR(CDCl₃): δ7.96(d, J=2.3Hz, 1H), 7.55(d, J=2.3 and 8.3Hz, 1H), 7.26(d, J=8.3Hz, 1H), 5.90(br s, 1H), 4.50(d, J=4.1Hz, 2H), 3.97(s, 3H), 2.44(sep, J=7.0Hz, 1H), 1.20(d, J= 7.0Hz, 6H); MS(ES⁺): 384.1 177 —OH

168 AE-1 ¹H NMR(DMSO-d₆): δ10.62(s, 1H), 8.88(m, 2H), 7.99(d, J=2.3Hz, 1H), 7.70(dd, J=2.3 and 8.5Hz, 1H), 7.06(d, J=8.7Hz, 1H), 4.09(m, 2H), 3.91(s, 3H), 2.70(m, 2H), 1.98(m, 1H, J= 6.8Hz), 0.93(d, J=6.8Hz, 6H); MS(ES⁺): 238.1 178 —OSO₂CF₃

177 B-2 ¹H NMR(CDCl₃): δ8.05(d, J=2.3Hz, 1H), 7.63(dd, J=2.3 and 8.3Hz, 1H), 7.25(d, J=8.3Hz, 1H), 3.96(s, 3H), 3.85(s, 2H), 2.43(d, J=6.8Hz, 2H), 1.77(m, J=6.6Hz; 1H), 0.93(d, J=6.6Hz, 1H); MS(ES⁺): 370.2 179 —OSO₂CF₃

178 R ¹H NMR(DMSO-d₆): δ7.93(m, 1H), 7.47(m, 1H), 7.26(m, 1H), 4.48(m, 2H), 3.96(s, 3H), 3.03(m, 2H), 1.91(m, 1H), 1.52(m, 9H), 0.89(d, J= 6.6Hz, 6H); MS(ES⁺): 492.2 (M + Na)⁺

No. Starting Method Cpd. —R —R′ From Used Analytical Data  7 —OBn —CHO 6 + 3a D-2 ¹H NMR(DMSO-d₆): δ□9.78(s, 1H), 8.85(t, J=5.7Hz, 1H), 8.50(d, J=2.0Hz, 1H), 8.20(dd, J=8.2, 1.9Hz, 1H), 7.55(m, 9H), 5.35(s, 2H), 3.69(s, 3H), 3.23(t, J=6.5Hz, 2H), 1.98(m, 1H), 1.02(d, J=6.8Hz, 6H); MS(ES⁺): 446.3  8 —OBn —CO₂H 7 E MS(ES⁺): 484.33 (M + Na)⁺  9 —OBn —CO₂MEM 8 F MS(ES⁺): 572.2 (M + Na)⁺ 10 —OH —CO₂MEM 9 G MS(ES⁺): 482.33 [(M − MEM) + Na]⁺ 11 —OSO₂CF₃ —CO₂MEM 10 B-2 ¹H NMR(DMSO-d₆): δ□8.75(t, J=5.6Hz, 1H), 8.44(d, J= 1.6Hz, 1H), 8.11(dd, J=8.0, 1.9Hz, 1H), 8.01(d, J=2.9Hz, 1H), 7.84(dd, J=8.4, 2.6Hz, 1H), 7.47(d, J=8.5Hz, 1H), 7.41(d, J= 8.0Hz, 1H), 5.23(q, AB system, 2H), 3.59(s, 3H), 3.44(m, 2H), 3.30(m, 2H), 3.18(s, 3H), 3.13(t, J=6.6Hz, 2H), 1.88(m, 1H), 0.91(d, J=6.7Hz, 6H); MS(ES⁺): 614.3 (M + Na)⁺ 29a

—CO₂MEM 11 D-3 Characterized in the next step 29b

—CO₂MEM 11 D-3 MS(ES⁺): 520.2 (M + Na)⁺ 29c

—CO₂MEM 11 D-3 MS(ES⁺): 482.3 29d

—CO₂MEM 11 D-3 MS(ES⁺): 562.3 (M + Na)⁺ 29e

—CO₂MEM 11 D-3 MS(ES⁺): 556.4 (M + Na)⁺ 29f

—CO₂MEM 11 D-3 ¹H NMR(DMSO-d₆): δ□8.50(t, J=5.6Hz, 1H), 8.18(d, J=1.9Hz, 1H), 7.86(dd, J=7.9, 1.9Hz, 1H), 7.78(d, J=1.7Hz, 1H), 7.56(dd, J=8.0, 1.8Hz, 1H), 7.13(d, J=8.0Hz, 1H), 7.00(d, J=7.9Hz, 1H), 6.67(dd, J=17.6, 11.1Hz, 1H), 5.76(d, J=17.6Hz, 1H), 5.19(d, J=11.1Hz, 1H), 4.99(q, AB system, 2H), # 3.37(s, 3H), 3.20(m, 2H), 3.11(m, 2H), 2.97(s, 3H), 2.91(t, J=6.7Hz, 2H), 1.67(m, 1H), 0.70(d, J=6.6Hz, 6H); MS(ES+): 492.3 (M + Na)⁺ 29g

—CO₂MEM 11 D-2 MS(ES⁺): 576.2 (M + Na)⁺; MS(ES⁻): 552.2 29h

—CO₂MEM 11 D-2 MS(ES⁺): 538.2 29i

—CO₂MEM 11 D-2 MS(ES⁺): 560.4 (M + Na)⁺ 30a

—CO₂H 29a I-1 MS(ES⁺): 398.3 ; MS(ES⁻): 396.3 30b

—CO₂H 29b I-1 Characterized in the next step 30c

—CO₂H 29c I-1 MS(ES⁻): 392.1 30d

—CO₂H 29d I-1 MS(ES⁺): 452.1 30e

—CO₂H 29e I-1 MS(ES⁺): 446.2 30f

—CO₂H 29f I-1 MS(ES⁻): 380.1 30g

—CO₂H 29g K, N, O, I-1 MS(ES⁺): 515.3 (M + Na)⁺; MS(ES⁻): 491.2 30h

—CO₂H 29h K, I-1 MS(ES⁻): 450.1 30i

—CO₂H 29i K, I-1 MS(ES⁻): 450.3 33 —OSO₂CF₃ —CO₂H 11 I-1 Characterized in the next step 41

—CO₂MEM 10 D-8 MS(ES⁻): 534.30 42

—CO₂H 41 I-1 MS(ES⁻): 446.30 48 —OCH₃ —CHO 47 + 3a D-2 MS(ES⁺): 392.2 (M + Na)⁺ 49 —OCH₃ —CO₂H 48 E MS(ES⁺): 386.1; 408.1 (M + Na)⁺

Cpd. Starting Method No. —R —R′ From Used Analytical Data 14 —OSO₂CF₃ —CHO 13 B-2 Characterized in the next step 15 —OSO₂CF₃ —CO₂H 14 E MS (ES⁻): 403.58 16 —OSO₂CF₃

15 A-3 or A-4 ¹HNMR(DMSO-d₆): δ□ 8.83(t, J=6Hz, 1H), 8.49(d, J=2.6Hz, 1H), 8.23(dd, J=8.6Hz, 1H), 7.72(d, J=8.6Hz, 1H), 7.49(m, 2H), 7.41(m, 3H), 5.43(s, 2H), 3.1(t, J=6.9Hz, 2H), 2.29(m, 1H), 0.89(d, J=6.9Hz, 6H).

Cpd. Starting Method No. —R —R′ From Used Analytical Data 17 —OBn —CHO 16 + 6 D-2 ¹HNMR(DMSO-d₆): δ□ 0.88(d, J=6.0Hz, 6H), 1.85(m, 1H), 3.1(t, J=6.0Hz, 2H), 5.02(q, J=13 and 2.5Hz, 2H), 5.18(s, 2H), 6.88(m, 2H), 7.17(d, J=8.6Hz, 1H), 7.26(m, 4H), 7.35 (m, 1H), 7.40(m, 4H), 7.49(d, J=7.7Hz, 2H), 8.07(dd, J=7.7 and 1.7Hz, 1H), 8.38(d, J=1.7Hz, 1H), 8.72(t, J=6Hz, 1H), 9.63(s, 1H); MS(ES+): 522.89 18 —OBn —CO₂H 17 E ¹HNMR(DMSO-d₆): δ□ 0.86(d, J=6.9Hz, 6H), 1.85(m, 1H), 3.09(t, J=6.9Hz, 2H), 5.01(d, J=5.01Hz, 2H), 5.14(s, 2H), 7.08(m, 3H), 7.14(dd, J=8.6 and 2.6Hz, 1H), 7.27(m, 4H), 7.34(m, 1H), 7.41(m, 3H), 7.48(m, 2H), 7.99(dd, J=6.9 and 1.8Hz, 1H), 8.32(s, 1H), 8.64(t, J=6Hz, 1H), 12.57(s, 1H); MS(ES+): 538.86 19 —OBn —CO₂MEM 18 F ¹HNMR(DMSO-d₆): δ 0.90(d, J=6.8Hz, 6H), 1.86(m, 1H), 3.10(t, J=6.5Hz, 2H), 3.16(s, 3H), 3.28(dd, J=3 and 6Hz, 2H), 3.36(dd, J=3 and 6Hz, 2H), 5.02(d, J=3.8Hz, 2H), 5.12 (d, J=15Hz, 2H), 5.64(s, 2H), 7.11(m, 3H), 7.24(dd, J=8.25 and 2.75Hz, 1H), 7.29(m, 4H), 7.35(m, 1H), 7.42(m, 3H), 7.49(m, 2H), 8.02(dd, J=1.7 and 8.2Hz, 1H), 8.36(d, 1.7Hz, 1H), 8.68(t, J=6Hz, 1H); MS(ES+): 626.44 21 —OH —CO₂MEM 19 G, H ¹HNMR(DMSO-d₆): δ 0.88(d, J=6Hz, 6H), 1.85(m, 1H) 3.10 (t, J=6Hz, 2H) 3.16(s, 3H), 3.28(m, 2H), 3.35(m, 2H), 5.04 (d, J=3.5Hz, 2H)5.11(d, J=14Hz, 2H), 6.98(m, 2H), 7.11 m, 2H), 7.29(m, 5H), 8.03(dd, J=8 and 2Hz, 1H), 8.32(d, J= 2Hz, 1H), 8.67(t, J=6Hz, 1H), 9.9(s, 1H); MS(ES+)536.30 (100%: M⁺¹) 22 —OSO₂CF₃ —CO₂MEM 21 B-2 ¹HNMR(DMSO-d₆): δ 0.89(d, J=6.8Hz, 6H), 1.86(m, 1H), 3.12(t, J=6.5Hz, 2H), 3.16(s, 3H), 3.29(m, 2H), 3.40(m, 2H), 5.04(s, 2H), 5.16(dd, J=18 and 6Hz, 2H), 7.15(m, 2H), 7.31(m, 3H), 7.36(d, J=8.5Hz, 1H), 7.41(d, J=8.5Hz, 1H), 7.73(dd, J=8.6 and 2.6Hz, 1H), 7.85(d, J=2.6Hz, 1H), 8.07 (dd, J=7.7 and 1.7Hz, 1H), 8.45(d, J=1.7Hz, 1H), 8.73(t, J= 6Hz, 1H); MS(ES+)668.15 24a

—CO₂MEM 22 + 23 D-1 ¹HNMR(DMSO-d₆): δ 0.89(d, J=6.8Hz, 6H), 1.87(m, 1H), 3.12(t, J=6Hz, 2H), 3.16(s, 3H), 3.29(m, 2H), 3.39(m, 2H), 5.05(d, J=2.6Hz, 2H), 5.16(d, J=17Hz, 2H), 7.08(m, 2H), 7.21(m, 4H), 7.24(d, J=7.7Hz, 1H), 7.35(d, J=7.7Hz, 1H), 7.62(d, J=3.5Hz, 1H), 7.64(d, J=5Hz, 1H), #7.86(d, J= 8.6Hz, 1H), 8.06(m, 2H), 8.42(s, 1H), 8.73(t, J=6Hz, 1H); MS (ES+)602.52 24b

—CO₂MEM 22 + 23 D-1 ¹HNMR(DMSO-d₆): δ 0.89(d, J=6.8Hz, 6H), 1.87(m, 1H), 3.12(t, J=6 and 6.8Hz, 2H), 3.16(s, 3H), 3.30(m, 2H), 3.39 (dd, J=5.2 and 3.4Hz, 2H), 5.04(d, J=4.3Hz, 2H), 5.16(d, J= 16Hz, 2H), 7.08(m, 2H), 7.20(m, 3H), 7.24(d, J=8.6Hz, 1H), 7.35(d, J=8.6Hz, 1H), 7.61(d, J=5Hz, 1H), 7.71(dd, J= 4.8 #and 3Hz, 1H), 7.91(dd, J=1.7 and 7.7Hz, 1H), 8.00(m, 1H), 8.06(dd, J=2 and 8Hz, 1H), 8.14(d, J=1.7Hz, 1H), 8.41 (d, J=1.7Hz, 1H), 8.68(t, J=6Hz, 1H); MS(ES+)602.27 24c

—CO₂MEM 22 + 23 D-1 ¹HNMR(DMSO-d₆): δ 0.89(d, J=6.8Hz, 6H), 1.87(m, 1H), 3.12(t, J=6 and 6.8Hz, 2H), 3.16(s, 3H), 3.30(m, 2H), 3.40 (m, 2H), 5.05(d, J=5Hz, 2H), 5.17(d, J=17Hz, 2H), 7.09(m, 2H), 7.21(m, 3H), 7.30(d, J=7.7Hz, 1H), 7.37(d, J=7.7Hz, 1H), 7.44(m, 1H), 7.54(t, J=7.7Hz, 2H), 7.73(d, J=6.8Hz, 2H), 7.88(dd, J=1.7 #and 7.7Hz, 1H), 8.07(dd, J=7.7 and 1.7 Hz, 1H), 8.11(d, J=1.7Hz, 1H), 8.42(d, J=1.7Hz, 1H), 8.72 (t, J=6Hz, 1H); MS(ES+)596.45 24d

—CO₂MEM 22 + 23 D-1 MS(ES+)616 24e

—CO₂MEM 22 + 23 D-1 MS(ES+)586.4 24f

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 586.39 24g

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 616.63 24h

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 597.25 24i

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 597.4 24j

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 597.4 24k

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 644.3 24l

—CO₂MEM 22 + 23 D-3 Characterized at the next step 24m

—CO₂MEM 22 + 23 D-10 Characterized at the next step 24n

—CO₂MEM 22 + 23 D-3 MS(ES⁺): 560.74 24o

—CO₂MEM 22 + 23 D-4 MS(ES⁺): 603.72 24p

—CO₂MEM 22 + 23 D-5 MS(ES⁺): 558.3 24q

—CO₂MEM 22 + 23 D-5 Characterized in the next step 24r

—CO₂MEM 22 + 23 D-5 MS(ES⁺): 610.4(M + Na)⁺ 24s

—CO₂MEM 22 + 23 D-3 Characterized in the next step 24t

—CO₂MEM 22 + 23 D-3 Characterized in the next step 24u

—CO₂MEM 22 + 23 D-3 MS(ES⁺): 598.4(M + Na)⁺ 24v

—CO₂MEM 22 + 23 D-3 MS(ES⁻): 500.4[(M − MEM) − 1]⁻ 24w

—CO₂MEM 22 + 23 D-5 Characterized in the next step 24x

—CO₂MEM 22 + 23 D-3 MS(ES⁺): 610.5(M + Na)⁺ 24y

—CO₂MEM 22 + 23 D-5 MS(ES⁺): 596.4(M + Na)⁺ 24z

—CO₂MEM 22 + 23 D-3 MS(ES⁺): 576.3(M + Na)⁺ 24aa

—CO₂MEM 22 + 23 D-11 Characterized in the next step 24ab

—CO₂MEM 22 + 23 D-2 MS(ES⁺): 630.55 24ac

—CO₂MEM 22 + 23 D-2 MS(ES⁺): 630.74 24ad

—CO₂MEM 22 + 23 D-2 MS(ES⁺): 652.3 24ae

—CO₂MEM 22 + 23 D-2 Characterized in the next step 24ag

—CO₂MEM 22 + 23 D-1 MS(ES⁺): 685.01 24ah

—CO₂MEM 22 + 23 D-3 MS(ES⁺): 546.49 25a

CO₂H 24a I-1 ¹HNMR(DMSO-d₆): δ 0.91(d, J=6.9Hz, 6H), 1.88(m, 1H), 3.13(t, J=6.9 and 6Hz, 2H), 5.07(d, J=11.2Hz, 2H), 7.09(m, 2H), 7.22(m, 5H), 7.35(d, 7.7Hz, 1H), 7.63(d, 2.6Hz, 1H), 7.65(d, J=5.2Hz, 1H), 7.82(dd, J=7.7 and 1.7Hz, 1H), 8.05 (d, J=1.7Hz, 1H), 8.07(s, 1H), 8.40(s, 1H), 8.72(t, J=6Hz, 1H), 12.77(brs, 1H); MS(ES+)514.19 25b

CO₂H 24b I-1 ¹HNMR(DMSO-d₆): δ 0.92(d, J=6.9Hz, 6H), 1.88(m, 1H), 3.12(t, J=6.9 and 6Hz, 2H), 5.07(d, J=13Hz, 2H), 7.09(m, 2H), 7.22(m, 4H), 7.35(d, J=8.6Hz, 1H), 7.63(d, J=5.2Hz, 1H), 7.70(dd, J=2.6 and 4.3Hz, 1H), 7.88(dd, J=7.2 and 1.7Hz, 1H), 8.02(d, J=1.7Hz, 1H), 8.07(dd, J=1.7 and 7.7Hz, 1H), 8.15(m, 1H), 8.39(d, #J=1.7Hz, 1H), 8.72(t, J=6Hz, 1H), 12.70(brs, 1H); MS(ES+)514.06 25c

CO₂H 24c I-1 ¹HNMR(DMSO-d₆): δ 12.73(bs, 1H), 8.73(t, J=6Hz, 1H), 8.41(d, J=1.7Hz, 1H), 8.12(d, J=1.7Hz, 1H), 8.07(dd, J= 7.7 & 1.7Hz, 1H),7.83(dd, J=7.7 & 1.7Hz, 1H), 7.72(d, J= 6.9Hz, 2H), 7.54(t, J=7.7, 2H), 7.44(t, J=7.7Hz, 1H), 7.37 (d, J=7.7 Hz, 1H), 7.28(d, J=7.7 Hz, 1H), 7.21(m, 3H), 7.09 (m, 2H), 5.08(d, #J=14Hz, 2H), 3.13(t, J=6.5Hz, 2H), 1.88 (m, 1H), 0.91(d, 6.8Hz, 6H); MS(ES+)507.93 25d

CO₂H 24d I-1 ¹HNMR(DMSO-d₆): δ 12.75(bs, 1H), 8.71(t, J=6Hz, 1H), 8.39(d, J=1.7Hz, 1H), 8.05(dd, J=1.7 & 7.7Hz, 1H), 8.01(d, J=2.5Hz, 1H), 7.75(dd, J=2.5 & 7.7Hz, 1H), 7.42(d, 3.4Hz, 1H), 7.34(d, J=7.7Hz, 1H), 7.22(m, 3H), 7.19(d, J=8.6Hz, 1H), 7.09(m, 2H), 6.95(d, J=3.4Hz, 1H), 5.06(d, J=11Hz, 2H), 3.12(t, #J=6.5Hz, 2H), 2.52(s, 3H), 1.89(m, 1H), 0.81(d, 6.8Hz, 6H); MS(ES+)528.51 25e

CO₂H 24e I-1 ¹HNMR(DMSO-d₆): δ 0.89(d, J=6Hz, 6H), 1.86(m, 1H), 3.12 (t, J=6.8 and 6.0Hz, 2H), 5.03(d, J=10Hz, 2H), 7.02(s, 1H), 7.06(m, 2H), 7.16(d, J=8.6Hz, 1H), 7.21(m, 3H), 7.31(d, J= 7.7Hz, 1H), 7.75(dd, J=8.5 and 1.7Hz, 1H), 7.78(t, J=1.7Hz, 1H), 8.04(m, 2H), 8.29(s, 1H), 8.36(d, J=1.7Hz, 1H), 8.66(t, J=6 and 5.2Hz, 1H), 12.58(bs, 1H); MS(ES+)498.49 25f

CO₂H 24f I-1 MS(ES⁺): 498.36 25g

CO₂H 24g I-1 ¹HNMR(DMSO-d₆): δ 12.72(bs, 1H), 8.69(t, J=6Hz, 1H), 8.39(d, J=1.7Hz, 1H), 8.06(m, 2H), 7.79(dd, J=1.7 & 7.7Hz, 1H), 7.45(s, 1H), 7.35(d, J=7.7Hz, 1H), 7.21(m, 5H), 7.1(m, 2H), 5.07(d, J=8.6Hz, 2H), 3.12(t, J=6.5Hz, 2H), 2.29(s, 3H), 1.89(m, 1H), 0.91(d, 6.8Hz, 6H); MS(ES+) 528.38 25h

CO₂H 24h I-1 ¹HNMR(DMSO-d₆): δ 12.74(bs, 1H), 8.73(m, 2H), 8.63(d, J= 1.7Hz, 1H), 8.41(d, J=1.7Hz, 1H), 8.23(dd, J=1.7 and 7.7Hz, 1H), 8.08(dd, J=1.7 & 7.7Hz, 1H), 8.05(d, J=7.7Hz, 1H), 7.96(dt, J=7.7 & 1.7Hz, 1H), 7.43(dd, J=6 & 7Hz, 1H), 7.37(d, J=7.7Hz, 1H), 7.29(d, J=8.6Hz, 1H), 7.18(m, 3H), 7.08(m, 2H), 5.01(q, J=10 & 25Hz, 2H), 3.13(t, #J=6.9 and 6Hz, 2H), 1.89(m, 1H), 0.92(d, J=6.9Hz, 6H); MS(ES+) 509.58 25i

CO₂H 24i I-1 ¹HNMR(DMSO-d₆): δ 12.70(bs, 1H), 8.91(d, J=2.6Hz, 1H), 8.68(t, J=6 & Hz, 1H), 8.62(d, J=2Hz, 1H), 8.4(d, J=1.7Hz, 1H), 8.12(m, 2H), 8.05(dd, J=8.6 & 1.7Hz, 1H), 7.88(d, 8.5 & 1.7Hz, 1H), 7.53(dd, J=8.6 & 5.2Hz, 1H), 7.34(d, J= 7.7Hz, 1H), 7.28(d, J=8.6Hz, 1H), 7.18(m, 3H), 7.08(m, 2H), 5.04(d, J=12Hz, 2H), 3.11(t, #J=6.5Hz, 2H), 1.87(m, 1H), 0.9(d, 6.8Hz, 6H); MS(ES+)509.11 25j

CO₂H 24j I-1 ¹HNMR(DMSO-d₆): δ 0.90(d, J=6.9Hz, 6H), 1.88(m, 1H), 3.1(t, J=6.9 and 6Hz, 2H), 5.03(s, 2H), 7.06(m, 2H), 7.18 (m, 3H), 7.33(d, 8.4Hz, 1H), 7.30(d, J=8.4Hz, 1H), 7.75(d, J = 6.2Hz, 2H), 7.85(m, 1H), 8.05(dd, J=7.6 and 1.7Hz, 1H), 8.18(s, 1H), 8.40(d, J=2Hz, 1H), 8.71(m, 4H); MS(ES+) 509.49 25k

CO₂H 24K I-1 Characterized in the next step 25l

CO₂H 24l I-1 MS(ES⁺): 511.54 25m

CO₂H 24m I-1 MS(ES⁺): 501.66 25n

CO₂H 24n I-1 MS(ES⁺): 472.4 25o

CO₂H 24o I-1 MS(ES⁺): 515.65 25p

CO₂H 24p I-1 Characterized in the next step 25q

CO₂H 24q I-1 MS(ES⁺): 536.3(M + Na)⁺ 25r

CO₂H 24r I-1 MS(ES⁻): 500.4 25s

CO₂H 24s I-1 Characterized in the next step 25t

CO₂H 24t I-1 Characterized in the next step 25u

CO₂H 24u I-1 MS(ES⁻): 486.4 25v

CO₂H 24v I-1 MS(ES⁺): 524.3(M + Na)⁺ 25w

CO₂H 24w I-1, Q Characterized in the next step 25x

CO₂H 24x I-1 MS(ES⁻): 498.3 25y

CO₂H 24y I-1 MS(ES⁻): 484.3 25z

CO₂H 24z I-1 MS(ES⁺): 488.3 25aa

CO₂H 24aa I-1 Characterized in the next step 25ab

CO₂H 24ab K, I-1 MS(ES⁺): 544.27 25ac

CO₂H 24ac K, I-1 MS(ES⁺): 544.2 25ad

CO₂H 24ad E, H, I-1 MS(ES⁺): 670.3(M + Na)⁺ 25ae

CO₂H 24ae K, I-1 ¹HNMR(DMSO-d₆): δ 9.1(bs, 2H), 8.8(bs, 2H), 8.5(t, J=6Hz, 1H), 8.02(s, 1H), 7.68(s, 1H), 7.62(m, 6H), 7.53(d, J=5.8Hz, 1H), 7.15(d, J=6Hz, 1H), ), 7.13(m, 1H), 7.01(s, 1H), 5.5(t, J=5Hz, 1H), 4.7(d, J=5Hz, 2H), 3.01(m, 2H), 1.8(m, 1H), 0.85(d, J=6.8Hz, 6H) 25af

CO₂H 24ad K, I-1 MS(ES⁺): 566.2(M + Na)⁺ 25ag

CO₂H 24ag I-1 MS(ES⁺): 597.7 25ah

CO₂H 24ah L, I-1 MS(ES⁺): 492.54 25ai

CO₂H 24ai L, M, K, N, O, I-1 Characterized in the next step

Cpd. Starting Method No. —R From Used Analytical Data 26a

25a J ¹HNMR(DMSO-d₆): δ 0.88(d, J=6.9Hz, 6H), 1.84(m, 1H), 3.07(t, J=6.9 and 6.0Hz, 2H), 5.05(s, 2H), 7.04(d, J=6.9Hz, 2H), 7.20(m, 4H), 7.35 (d, J=7.7Hz, 1H), 7.43(d, J=7.7Hz, 1H), 7.66(d, J=5.2Hz, 1H), 7.70 (d, J=4.3Hz, 1H), 7.75(m, 4H), 7.82(dd, J=7.7 and 1.7Hz, 1H), 7.94(d, J=1.7Hz, 1H), 8.03(dd, J=7.7 and 1.7Hz, 1H), 8.26(dd, J=7.7. and # 1.7Hz, 1H), 8.69(t, J=6Hz, 1H), 8.80(s, 2H), 9.17(s, 2H), 10.76(s, 1H); MS(ES+)631.05 26b

25b J ¹HNMR(DMSO-d₆): δ 0.88(d, J=6.9Hz, 6H), 1.84(m, 1H), 3.07(t, J=6.8 and 6.0Hz, 2H), 5.04(s, 2H), 7.02(d, J=6.8Hz, 2H), 7.20(m, 3H), 7.34 (d, J=7.7Hz, 1H), 7.43(d, J=8.6Hz, 1H), 7.72(m, 6H), 7.90(dd, J=1.7 and 7.7Hz, 1H), 8.05(m, 3H), 8.23(d, J=1.7Hz, 1H), 8.68(t, J=6 and 5.2Hz, 1H), 8.82(s, 2H), 9.17(s, 2H), 10.73(s, 1H); MS(ES+)631.82 26c

25c J ¹HNMR(DMSO-d₆): δ 10.75(s, 1H), 9.19(s, 2H), 8.89(s, 2H), 8.69(t, J=6Hz, 1H), 8.29(d, J=1.7Hz, 1H), 8.07(dd, J=7.7 & 1.7Hz, 1H), 7.99(d, J=1.7Hz, 1H), 7.87(dd, J=7.7 & 1.7Hz, 1H), 7.83(d, J=7.7Hz, 2H), 7.77(m 5H), 7.54(t, J=7.7, 2H), 7.43(m, 3H), 7.19(m, 3H), 7.03(d, J=6.9Hz, 2H), 5.04(bs, 2H), 3.09(t, J=6.5Hz, 2H), 1.84(m, 1H), # 0.89(d, 6.8Hz, 6H); MS(ES+)625.81 26d

25d J ¹HNMR(DMSO-d₆): δ 10.7(s, 1H), 9.14(s, 2H), 8.82(s, 2H), 8.64(t, J=6Hz, 1H), 8.21(s, 1H), 7.98(dd, J=7.8 & 2Hz, 1H), 7.8(d, J=2Hz, 1H), 7.7(m, 4H), 7.68(dd, J=2 & 7.8Hz, 1H), 7.44(d, J=3Hz, 1H), 7.37(d, 7.8Hz, 1H), 7.27(d, J=7.7Hz, 1H), 7.16(m, 3H), 7.0(s, 1H), 6.99(s, 1H), 6.86(d, J=3Hz, 1H), 5.0(s, 2H), 3.03(t, J=6.5Hz, 2H), 2.46(s, 3H), # 1.78(m, 1H), 0.83(d, 6.8Hz, 6H); MS(ES+)645.77 26e

25e J ¹HNMR(DMSO-d₆): δ 0.87(d, J=6.2Hz, 6H), 1.73(m, 1H), 3.07(t, J=6.7 and 6.2Hz, 2H), 5.05(s, 2H), 7.03(dd, J=1.7 and 8Hz, 2H), 7.11(d, J 1.7Hz, 1H), 7.21(m, 3H), 7.31(d, J=8Hz, 1H), 7.42(d, J=8Hz, 1H), 7.78 (m, 5H), 7.92(d, J=1.7Hz, 1H), 8.02(dd, J=8 and 1.7Hz, 1H), 8.25(d, J=1.9Hz, 1H), 8.33(s, 1H), 8.63(t, J=6 and 5Hz, 1H), 8.80(bs, 2H), 9.14 #(bs, 2H), 10.67(s, 1H); MS(ES+)615.75 26f

25f J ¹HNMR(DMSO-d₆): δ 0.87(d, J=6.7Hz, 6H), 1.83(m, 1H), 3.06(t, J=6.7 and 6.2Hz, 2H), 5.04(s, 2H), 6.67(m, 1H), 7.03(m, 2H), 7.16(m, 3H), 7.35(d, J=8.6Hz, 1H), 7.42(d, J=8Hz, 1H), 7.74(m, 4H), 7.85(m, 2H), 7.98(d, J=1.2Hz, 1H), 8.03(dd, J=1.7 and 8Hz, 1H), 8.25(d, J=1.8Hz, 1H), 8.67(t, J=6.2 and 5.5Hz, 1H), 8.88(bs, 2H), # 9.12(bs, 2H), 10.772(bs, 1H); MS(ES+)615.75 26g

25g J ¹HNMR(DMSO-d₆): δ 10.67(s, 1H), 9.12(s, 2H), 8.78(s, 2H), 8.61(t, J=6Hz, 1H), 8.21(s, 1H), 7.98(dd, J=7.8 & 2Hz, 1H), 7.84(d, J=2Hz, 1H), 7.7(m, 5H), 7.46(s, 1H), 7.39(d, 7.8Hz, 1H), 7.29(d, J=7.7Hz, 1H), 7.16 (m, 4H), 7.01(s, 1H), 6.99(s, 1H), 5.0(s, 2H), 3.03(t, J=6.5Hz, 2H), 2.23 (s, 3H), 1.79(m, 1H), 0.83(d, 6.8Hz, 6H); MS(ES+)645.77 26h

25h J ¹HNMR(DMSO-d₆): δ 10.77(bs, 1H), 8.95(bs, 4H), 8.76(d, J=4.3Hz, 1H), 8.69(t, J=6Hz, 1H), 8.4(s, 1H), 8.29(m, 2H), 8.15(d, J=7.7Hz, 1H), 8.07(dd, J=1.7 and 7.7Hz, 1H), 7.99(dt, J=1.7 & 7.7Hz, 1H), 7.76(m, 4H), 7.46(m, 2H), 7.18(m, 3H), 7.05(s, 1H), 7.03(s, 1H), 5.06(s, 2H), 3.10 (t, J=6.9 and 6Hz, 2H), # 1.86(m, 1H), 0.89(d, J=6.9Hz, 6H); MS(ES+)626.69 26i

25i J ¹HNMR(DMSO-d₆): δ 10.73(bs, 1H), 9.16(bs, 2H), 9.05(d, J=1.9Hz, 1H), 8.79(s, 2H), 8.69(t, J=6 & Hz, 1H), 8.64(dd, J=1.2 & 5Hz, 1H), 8.29(d, J=1.7Hz, 1H), 8.24(d, J=8Hz, 1H), 8.05(m, 2H), 7.93(dd, 8 & 1.8Hz, 1H), 7.76(m, 5H), 7.56(dd, J=8 & 4.3Hz, 1H), 7.44(d, J=7.4Hz, 2H), 7.18(m, 3H), 7.0(m, 2H), 5.0(s, 2H), 3.08(t, J=6.5Hz, 2H), 1.82 #(m, 1H), 0.88(d, 6.8Hz, 6H);; MS(ES+)626.44 26j

25j J ¹HNMR(DMSO-d₆): δ 0.87(d, J=6.9Hz, 6H), 1.75(m, 1H), 3.08(t, J=6.9 and 6.0Hz, 2H), 5.03(s, 2H), 7.03(m, 1H), 7.18(m, 3H), 7.45(t, J=7.8 and 7Hz, 2H), 7.76(s, 4H), 7.87(d, J=6Hz, 2H), 7.94(dd, J=8 and 2Hz, 1H), 8.05(dd, J=8 and 2Hz, 1H), 8.08(d, J=2Hz, 1H), 8.29(d, J=2Hz, 1H), 8.70(m, 3H), 8.84(s, 2H), 9.11(s, 2H), 10.76(s, 1H); MS(ES+)626.76 26k

25k J ¹HNMR(DMSO-d₆): δ 10.72(bs, 1H), 9.15(bs, 2H), 8.81(bs, 2H), 8.86(t, J=6Hz, 1H), 8.28(s, 1H), 8.03(m, 3H), 7.91(d, J=7.9Hz, 1H), 7.81(d, J=4Hz, 1H), 7.74(s, 4H), 7.42(d, J=7.9Hz, 1H), 7.38(d, J=7.9Hz, 1H), 7.18(m, 3H), 7.04(m, 2H), 5.04(bs, 2H), 3.07(t, J=6Hz, 2H), 2.57(s, 3H), 1.83(m, 1H), 0.87(d, J=6.8Hz, 6H); MS(ES+)673.7 26l

25l J ¹HNMR(DMSO-d₆): δ 10.66(s, 1H), 9.20(s, 2H), 8.86(s, 2H), 8.66(t, J=6Hz, 1H), 8.24(d, J=2Hz, 1H), 8.15(dd, J=7.8 & 2Hz, 1H), 7.69(m, 4H), 7.68(d, J=Hz, 1H), 7.63(d, J=7.9Hz, 1H), 7.43(d, J=7.9Hz, 1H), 7.37 (d, J=7.9Hz, 1H), 7.24(m, 3H), 7.09(m, 2H), 6.92(s, 1H), 6.40(s, 1H), 6.17(t, J=4Hz, 1H), # 5.10(bs, 2H), 3.74(s, 3H), 3.09(t, J=6Hz, 2H), 1.83(m, 1H), 0.88(d, J=6.8Hz, 6H); MS(ES+)628.65 26m

25m J MS(ES+): 618.91 26n

25n J ¹HNMR(DMSO-d₆): δ 10.56(s, 1H), 9.15(bs, 2H), 8.84(bs, 2H), 8.64(t, J=6Hz, 1H), 8.19(d, J=2Hz, 1H), 7.99(d, J=7Hz, 1H), 7.70(m, 4H), 7.46(s, 1H), 7.36(m, 2H), 7.24(m, 3H), 7.05(s, 1H), 7.00(s, 1H), 6.0(m, 1H), 5.18(d, J=16Hz, 1H), 5.10(d, J=11Hz, 1H), 5.0(s, 2H), 3.47(d, J=6Hz, 1H), # 3.03(t, J=6Hz, 2H), 1.79(m, 1H), 0.83(d, J=6.8Hz, 6H); MS(ES+)589.5 26o

25o J ¹HNMR(DMSO-d₆): δ 10.84(s, 1H), 9.16(s, 2H), 8.78(s, 2H), 8.69(t, J=6Hz, 1H), 8.27(d, J=2Hz, 1H), 8.19(s, 1H), 8.09(dd, J=2 & 7.7Hz, 1H), 8.04(dd, J=2 & 7.7Hz, 1H), 8.01(d, J=4Hz, 1H), 7.89(d, J=3Hz, 1H), 7.73(m, 4H), 7.44(dd, J=3 & 7.8Hz, 2H), 7.16(m, 3H), 7.30(s, 1H), 7.05 (s, 1H), 5.03(bs, 2H), # 3.06(t, J=6.5Hz, 2H), 1.82(m, 1H), 0.86(d, 6.8Hz, 6H); MS(ES+)632.4 26p

25p J MS(ES⁺): 609.3(M+Na)⁺ 26q

25q J MS(ES+)631.5 26r

25r J ¹HNMR(DMSO-d₆): δ 10.71(s, 1H), 9.16(s, 2H), 8.81(s, 2H), 8.68(t, J=6Hz, 1H), 8.25(s, 1H), 8.03(d, J=7.8Hz, 1H), 7.73(m, 5H), 7.69(s, 1H), 7.55(d, J=7.8Hz, 1H), 7.39(d, J=8.9Hz, 1H), 7.26(m, 3H), 7.03(m, 2H), 5.02(bs, 2H), 4.95(t, J=5Hz, 1H), 3.62(q, J=6 & 12.8Hz, 2H), 3.07 (t, J=6Hz, 2H), # 2.62(t, J=6Hz, 2H), 1.83(m, 1H), 0.88(d, J=6.8Hz, 6H); MS(ES+)617.4 26s

25s J ¹HNMR(DMSO-d₆): δ 0.89(d, J=6.8Hz, 6H), 1.84(m, 1H), 1.99(s, 3H), 3.09(t, J=6Hz, 2H), 5.04(s, 2H), 5.18(s, 1H), 5.28(s, 1H), 6.73(d, J=16Hz, 1H), 7.04(d, J= 6Hz, 2H), 7.23(m, 5H), 7.42(d, J=9Hz, 1H), 7.73 (m, 5H), 7.85(s, 1H), 8.03(dd, J=9 and 2Hz, 1H), 8.26(d, J=2Hz, 1H), 8.69(t, J=6Hz, 1H), # 8.87(bs, 4H), 10.91(s, 1H); MS(ES+)615.4 26t

25t J ¹HNMR(DMSO-d₆): δ 10.8(br s, 1H), 9.1 and 8.9(2 br s, 4H), 8.6(m, 1H), 8.2(s, 1H), 8.0(m, 1H), 7.8-7.6(m, 6H), 7.40(, J=6.9Hz, 1H), 7.3(m, 4H), 7.0(d, 1H), 5.6(m, 1H), 5.2(m, 1H), 5.0(br s, 1H), 3.1(t, J=6.8Hz, 2H), 2.2(s, 3H), 1.8(m, 1H), 0.95(d, 6H); MS(ES+)589.4, MS(ES−)587.5 26u

25u J ¹HNMR(DMSO-d₆): δ 0.88(d, J=6.8Hz, 6H), 1.84(m, 1H), 3.09(t, J=6Hz, 2H), 4.33(t, J=5.5Hz, 2H), 5.02(s, 2H), 5.01(t, J=5.5Hz, 1H), 5.95 (m, 1H), 6.57(d, J=11.5Hz, 1H), 7.04(d, J=6.7Hz, 2H), 7.25(m, 3H), 7.31(d, J=7.8Hz, 1H), 7.43(m, 2H), 7.54(s, 1H), 7.74(s, 4H), 8.05(dd, # J=7.8 and 2Hz, 1H), 8.23(d, J=2Hz, 1H), 8.69(t, J=6Hz, 1H), 8.83(bs, 2H), 9.18(bs, 2H), 10.66(s, 1H); MS(ES+)605.3 26v

25v J ¹HNMR(DMSO-d₆): δ 0.88(d, J=6.8Hz, 6H), 1.84(m, 1H), 2.75(t, J=7Hz, 2H), 3.09(t, J=6Hz, 2H), 3.60(m, 2H), 4.65(t, J=5Hz, 1H), 5.05(s, 2H), 7.05(d, J=7Hz, 2H), 7.29(m, 5H), 7.42(d, J=7.8Hz, 1H), 7.66(dd, J=7.8 and 2Hz, 1H), 7.75(m, 6H), 8.03(dd, J=7.8 and 2Hz, 1H), 8.25(s, 1H), # 8.68(t, J=6Hz, 1H), 8.82(bs, 2H), 9.18(bs, 2H), 10.68(s, 1H); MS(ES+)619.4 26w

25w J ¹HNMR(DMSO-d₆): δ 0.88(d, J=6.8Hz, 6H), 1.84(m, 1H), 3.09(t, J=6Hz, 2H), 4.41(s, 1H), 5.04(d, J=11Hz, 2H), 7.05(d, J=5.5Hz, 2H), 7.29 (m, 3H), 7.34(d, J=8Hz, 1H), 7.40(d, J=8Hz, 1H), 7.65(dd, J=8 and 2Hz, 1H), 7.75(s, 4H), 7.79(s, 1H), 8.05(dd, J=8 and 2Hz, 1H), # 8.28(d, J=2Hz, 1H), 8.71(t, J=6Hz, 1H), 8.82(bs, 2H), 9.17(bs, 2H), 10.73(s, 1H); MS(ES+)573.3 26x

25x J ¹HNMR(DMSO-d₆): δ 0.86(d, J=6.8Hz, 6H), 1.47(s, 3H), 1.74(s, 3H), 1.85(m, 1H), 3.06(t, J=6Hz, 2H), 3.43(d, J=8Hz, 1H), 5.04(s, 2H), 5.11(m, 1H), 7.03(m, 2H), 7.23(m, 5H), 7.52(m, 2H), 7.72(m, 5H), 8.02 (m, 1H), 8.21(s, 1H), 8.66(t, J=6Hz, 1H), 8.81(bs, 2H), 9.23(bs, 2H), 10.52(s, 1H); MS(ES+)617.6 26y

25y J ¹HNMR(DMSO-d₆): δ 0.87(d, J=6.8Hz, 6H), 1.72(m, 1H), 3.07(t, J=6Hz, 2H), 4.36(d, J=6Hz, 2H), 5.0(m, 2H), 5.42(t, J=6Hz, 1H), 7.03(d, J=7Hz, 2H), 7.25(m, 3H), 7.31(d, J=8Hz, 1H), 7.39(d, J=8Hz, 1H), 7.58 (d, J=8Hz, 1H), 7.73(m, 5H), 8.02(dd, J=10 and 2Hz, 1H), 8.23(s, 1H), # 8.68(t, J=6Hz, 1H), 8.76(bs, 2H), 9.15(bs, 2H), 10.71(s, 1H); MS(ES+)603.4 26z

25z J ¹HNMR(DMSO-d₆): δ 10.6(s, 1H), 9.17(s, 1H), 8.85(s, 1H), 8.68(d, J=5.9Hz, 2H), 8.25(d, 1.98Hz, 1H), 8.05(d, J=1.96Hz, 1H), 8.03(d, J=1.9Hz, 1H), 7.75(m, 4H), 7.65(m, 4H), 7.41(d, J=7.87Hz, 4H), 7.25(m, 1H) 5.4(s, 1H), 5.2(d, J=5.9Hz, 2H), 4.44(d, J=5.9Hz, 1H), 3.09(d, # J=6.89Hz, 2H), 1.89(d, J=6.89Hz, 2H) 0.88(d, J=5.9Hz, 6H); MS(ES+)605.69 26aa

25aa J Characterized in the next step 26ab

26ab J ¹HNMR(DMSO-d₆): δ 10.70(s, 1H) 9.15(bs, 2H), 8.77(bs, 2H), 8.67(t, J=6Hz, 1H), 8, 25(s, 1H), 8.04(d, J=7Hz, 1H), 7.77(d, J=2Hz, 1H), 7.71 (m 4H), 7.70(d, J=2Hz, 1H), 7.59(d, J=6Hz, 1H), 7.46(d, J=8Hz, 1H), 7.41(d, J=8Hz, 1H), 7.22(m, 3H), 7.05(s, 1H), 7.03(d, J=2Hz, 1H), 5.31(t, J=6Hz, 1H), # 5.04(bs, 2H), 4.51(d, J=6Hz, 2H), 3.07(t, J=6Hz, 2H), 1.82(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES+)661.74 26ac

25ac J ¹HNMR(DMSO-d₆): δ 0.87(d, J=6.8Hz, 6H), 1.83(m, 1H), 3.07(t, J=6Hz, 2H), 4.71(d, J=5Hz, 2H), 5.04(bs, 2H), 5.69(t, J=5Hz, 1H), 7.03 (d, J=5.8Hz, 2H), 7.21(m, 3H), 7.35(d, J=5Hz, 1H), 7.38(d, J=8Hz, 1H), 7.44(m, d, J=8Hz, 1H), 7.58(d, J=5Hz, 1H), 7.74(m, 6H), 8.03(d, J=8Hz, 1H), # 8, 24(s, 1H), 8.67(t, J=6Hz, 1H), 8.79(bs, 2H), 9.14(bs, 2H), 10.64(s, 1H); MS(ES+)661.74 26ad

25ad J ¹HNMR(DMSO-d₆): δ 9.65(s, 1H), 8.71(t, J=5.15Hz, 1H) 8.39(d, J=2.57Hz, 4H), 8.09(d, J=1.79Hz, 4H), 8.05(d, J=1.79Hz, 4H), 7.43(d, J=7.77Hz, 2H), 7.29(s, 2H), 7.19(m, 2H), 7.08(m, 2H), 5.03(d, J=2.58Hz, 2H) 3.29(m, 2H), 3.12(s, 4H), 2.49(m, 2H), 1.87(m, 2H), 0.90(d, J=6.87Hz, 6H); MS(ES+)765.4 26ae

25ae J ¹HNMR(DMSO-d₆): δ 9.1(bs, 2H), 8.8(bs, 2H), 8.5(t, J=6Hz, 1H), 8.02 (s, 1H), 7.68(s, 1H), 7.62(m, 6H), 7.53(d, J=5.8Hz, 1H), 7.15(d, J=6Hz, 1H), ), 7.13(m, 1H), 7.01(s, 1H), 5.5(t, J=5Hz, 1H), 4.7(d, J=5Hz, 2H), 3.01(m, 2H), 1.8(m, 1H), 0.85(d, J=6.8Hz, 6H); MS(ES+)571.2 26af

25af J ¹HNMR(DMSO-d₆): δ 10.6(s, 1H), 9.17(s, 1H), 8.85(s, 1H), 8.68(d, J=5.9Hz, 2H), 8.25(d, 1.98Hz, 1H), 7.75(m, 4H), 7.65(m, 4H), 7.41(d, J=7.87Hz, 4H), 7.25(m, 4H), 5.4(s, 1H), 5.2(d, J=5.9Hz, 2H), 4.44(d, J=5.9Hz, 1H), 3.09(d, J=6.89Hz, 2H), 1.89(d, J=6.89Hz, 2H), 0.88(d, J=5.9Hz, 6H). 26ag

25ag J ¹HNMR(DMSO-d₆): δ 0.90(d, J=6.9Hz, 6H), 1.41(s, 9H), 1.87(m, 1H), 3.11(t, J=6.9 and 6Hz, 2H), 5.07(s, 2H), 6.37(t, J=3.4Hz, 1H), 6.51(s, 1H), 7.11(m, 2H), 7.26(m, 3H), 7.33(d, 7.7Hz, 1H), 7.41(d, J=8.6Hz, 1H), 7.45(d, J=1.7Hz, 1H), 7.61(dd, J=1.7 and 7.7, 1H), 7.74(m, 5H), 8.05(dd, J=8.6 and 1.7Hz, 1H), 8.26(d, # J=1.7Hz, 1H), 8.66(t, J=5 and 6 Hz, 1H), 8.77(bs, 2H), 9.15(bs, 2H), 10.58(s, 1H); MS(ES+)714.78 26ah

25ah J MS(ES⁺):609.6 26ai

25ai J ¹HNMR(DMSO-d₆): δ 10.8(s, 1H), 6.2 and 8.9(2br s, 2H each, 4H), 8.7(t, 1H), 8.2(s, 1H), 8.0(d, J=6Hz, 1H), 7.7(m, 5H), 7.6(d, J=5Hz, 1H), 7.4(d, J=5.8Hz, 1H), 7.35(d, J=6.9Hz, 1H), 7.29(m, 3H), 7.0(m, 2H), 5.0(m, 2H), 4.6(s, 2H), 3.01(t, J=6.8Hz, 2H), 1.81(m, 1H), 0.95(d, J=6.8Hz, 6H); MS(ES+)604.3

Cpd. Starting Method No. —R —R¹ From Used Analytical Data 27a

26a I-2 ¹H NMR (DMSO-d₆): δ 14.95(s, 1H), 8.97(s, 4H), 8.5 (t, J=6Hz, 1H), 7.97(d, J=2Hz, 1H), 7.80(d, J=2 Hz, 1H), 7.73(dd, J=7.9 and 2Hz, 1H), 7.61(m, 7H), 7.18(t, J=3.9Hz, 1H), 7.05(d, J=7.9Hz, 1H), 6.93 (d, J=7.9Hz, 1H), 3.01(t, J=6.9 and 6.0Hz, 2H), 1.81 (m, 1H), 0.84(d, J=6.9Hz, 6H); MS (ES⁺): 541.17 27b

26b I-2 ¹H NMR (DMSO-d₆): δ 13.24(s, 1H), 9.05(s, 2H), 8.9 (s, 2H), 8.49(t, J=6 and 5.2Hz, 1H), 7.97(s, 1H), 7.99 (s, 1H), 7.87(s, 1H), 7.75(d, J=7.7Hz, 1H), 7.65(m, 1 H), 7.62(m, 6H), 7.05(d, J=7.7Hz, 1H), 6.93(d, J = 7.7Hz, 1H), 3.01(t, J=6.9 and 6.0Hz, 2H), 1.81(m, 1 H), 0.85(d, J=6.9Hz, 6H); MS (ES⁺): 541.42 27c

26c I-2 ¹H NMR (DMSO-d₆): δ 13.28(s, 1H), 9.04(s, 4H), 8.5 (t, J=6Hz, 1H), 7.97(s, 1H), 7.82(s, 1H), 7.74(m, 3 H), 7.62(m, 5H), 7.5(t, J=7.7Hz, 2H), 7.4(t, J=7.7, 1H), 7.1(d, J=7.7Hz, 2H), 6.97(d, J=7.7.Hz, 1H), 3.01(t, J=6.5Hz, 2H), 1.8(m, 1H), 0.85(d, 6.8Hz, 6 H); MS (ES⁺): 535.48 27d

26d I-2 ¹H NMR (DMSO-d₆): δ 9.03(s, 2H), 8.89(s, 2H), 8.49 (t, J=6Hz, 1H), 7.99(s, 1H), 7.65(m, 8H), 7.37(d, J= 3Hz, 1H), 7.04(d, J=7.7Hz, 1H), 6.98(s, 1H), 6.82 (d, J=3Hz, 1H), 2.98(t, J=6.5Hz, 2H), 2.46(s, 3H), 1.76(m, 1H), 0.81(d, 6.8Hz, 6H); MS (ES⁺): 555.61 27e

26e I-2 ¹H NMR (DMSO-d₆): δ 14.10(s, 1H), 9.05(bs, 2H), 8.79(bs, 2H), 8.47(t, J=5.6Hz, 1H), 8.3(s, 1H), 7.96 (d, J=2Hz, 1H), 7.78(m, 1H), 7.63(m, 7H), 7.05(m, 1H), 7.01(d, J=7.7Hz, 1H), 6.92(d, J=7.7Hz, 1H), 3.02(t, J=4.9Hz, 2H), 1.81(m, 1H), 0.85(d, J=6.3 Hz, 6H); MS (ES⁺): 525.36 27f

26f I-2 ¹H NMR (DMSO-d₆): δ 9.07(s, 2H), 8.86(s, 2H), 8.53 (t, J=5Hz, 1H), 8.03(s, 1H), 7.89(d, J=1.4Hz, 1H), 7.78(m, 2H), 7.65(m, 6H), 7.1(m, 2H), 7.08(d, J=7 Hz, 1H), 6.64(dd, J=3.5 and 2Hz, 1H), 3.03(t, J=6.9 and 6.0Hz, 2H), 1.81(m, 1H), 0.86(d, J=6.9Hz, 6H); MS (ES⁺): 525.43 27g

26g I-2 ¹H NMR (DMSO-d₆): δ 13.81(s, 1H), 8.74(bs, 4H), 8.43(t, J=6Hz, 1H), 7.92(d, J=2Hz, 1H), 7.69(d, J= 2Hz, 1H), 7.62(dd, J=7.7 & 2Hz, 1H), 7.54(m, 5H), 7.38(s, 1H), 7.15(s, 1H), 6.99(d, J=7.8Hz, 1H), 6.89 (d, J=6.8Hz, 1H), 2.97(t, J=6.5Hz, 2H), 2.20(s, 3 H), 1.76(m, 1H), 0.8(d, 6.8Hz, 6H); MS (ES⁺): 555.67 27h

26h I-2 ¹H NMR (DMSO-d₆): δ 13.95(bs, 1H), 8.99(bs, 2H), 8.79(bs, 2H), 8.65(d, J=5Hz, 1H), 8.43(t, J =6Hz, 1 H), 8.25(s, 1H), 8.09(d, J=7.8Hz, 1H), 8.00(d, J= 7.8 Hz, 1H), 7.94(s, 1H), 7.87(t, J=7.8Hz, 1H), 7.58 (m, 5H), 7.34(dd, J=7.8 & 5Hz, 1H), 7.09(dd, J=7.7 Hz, 1H), 6.90(d, J=7.8Hz, 1H), 2.97(t, J=5Hz, 2H), 1.76(m, 1H), 0.81(d, 6.8Hz, # 6H); MS (ES⁺): 268.64 (m/2) 27i

26i I-2 ¹H NMR (DMSO-d₆): δ 9.05(bs, 2H), 8.95(d, J= Hz, 1H), 8.75(s, 2H), 8.65(dd, J=5 & 1.4Hz, 1H), 8.5 (t, J=5.6Hz, 1H), 8.2(dt, J=1.8 & 7.7Hz, 1H), 7.99 (d, J=2.1Hz, 1H), 7.9(d, J=2.1Hz, 1H), 7.85(dd, J= 7.7 & 2.2Hz, 2H), 7.65(m, 5H), 7.55(dd, J=7.7 & 4.5 Hz, 1H), 7.15(d, J=7.7Hz, 1H), 6.95(d, J=7.7Hz, 1 H), 3.08(t, J=5Hz, 2H), # 1.82(m, 1H), 0.9(d, 6.8Hz, 6 H); MS (ES⁺): 268.85 (m/2) 27j

26j I-2 ¹H NMR (DMSO-d₆): δ 14.19(s, 1H), 9.06(bs, 2H), 8.67(bs, 2H), 8.67(d, J=6Hz, 2H), 8.50(t, J=6Hz, 1 H), 7.97(m, 2H), 7.91(dd, J=7.7 and 2Hz, 1H), 7.80 (d, J=6Hz, 2H), 7.64(m, 6H), 7.18(d, J=7.7Hz, 1 H), 6.95(d, J=7.7Hz, 1H), 3.02(t, J=5.0Hz, 2H), 1.82(m, 1H), 0.80(d, J=6.9Hz, 6H); MS (ES⁺): 536.43 27k

26k I-2 ¹H NMR (DMSO-d₆): δ 9.04(bs, 2H), 8.78(bs, 2H), 8.55(t, J=6Hz, 1H), 8.1(s, 1H), 7.98(d, J=4Hz, 1 H), 7.95(s, 1H), 7.87(d, J=7.9Hz, 1H), 7.75(d, J= 6.9Hz, 1H), 7.66(m, 4H), 7.2(m, 2H), 7.09(s, 1H), 3.03(t, J=6Hz, 2H), 2.55(s, 3H), 1.81(m, 1H), 0.85 (d, J=6.8Hz, 6H); MS (ES⁺): 583.59 27l

26l I-2 ¹H NMR (DMSO-d₆): δ 9.1(s, 2H), 8.84(s, 2H), 8.56(t, J=6Hz, 1H), 8.08(bs, 1H), 7.67(m, J=7H), 7.58(d, J= 7.9Hz, 1H), 7.11(m, 2H), 6.91(bs, 1H), 6.31(bs, 1 H), 6.11(t, J=3Hz, 1H), 3.74(s, 3H), 3.05(t, J=6Hz, 2H), 1.83(m, 1H), 0.88(d, J=6.8Hz, 6H); MS (ES⁺): 538.64 27m

26m I-2 ¹H NMR (DMSO-d₆): δ 9.04(s, 2H), 8.94(s, 2H), 8.46 (t, J=6Hz, 1H), 7.96(s, 1H), 7.63(m, 6H), 6.94(s, 1 H), 6.83(d, J=7.7Hz, 1H), 6.7(d, J=2, 1H), 6.62(dd, J=7.7 and 2Hz, 1H), 3.28(m, 4H), 3.02(t, J=6.5Hz, 2H), 1.98(m, 4H), 1.82(m, 1H), 0.82(d, 6.8Hz, 6H); MS (ES⁺): 528.76 27n

26n I-2 ¹H NMR (DMSO-d₆): δ 13.96(s, 1H), 9.02(s, 2H), 8.85 (s, 2H), 8.46(t, J=6Hz, 1H), 7.91(s, 1H), 7.58(m, 4 H), 7.39(s, 1H), 7.25(d, J=7.8Hz, 1H), 6.92(d, J= 7.7, 1H), 6.87(d, J=7.7Hz, 1H), 6.01(m, 1H), 5.17(d, J=16.7Hz, 1H), 5.08(d, J=10Hz, 1H), 3.45(d, J=6 Hz, 2H), 2.99(t, J=6Hz, 2H), 1.78(m, 1H), 0.83(d, J= 6.8Hz, 6H); MS # (ES⁺): 499.3 27o

26o I-2 ¹H NMR (DMSO-d₆): δ 14.08(bs, 1H), 9.06(s, 2H), 8.79(s, 2H), 8.51(t, J=6Hz, 1H), 8.11(d, J=2Hz, 1 H), 8.01(m, 3H), 7.85(d, J=3Hz, 1H), 7.63(m, 6H), 7.17(d, J=7.8Hz, 1H), 6.97(d, J=7.8Hz, 1H), 3.02 (t, J=6.5Hz, 2H), 1.81(m, 1H), 0.86(d, 6.8Hz, 6H); MS (ES⁺): 542.2) 27p

26p I-2 ¹H NMR (DMSO-d₆): δ 9.1 and 9.2(2 br s, 4H, NH proton), 8.6(m, 1H), 8.3(m, 1H), 8.0-7.6(m, 8H, aromatic proton), 7.3(m, 2H), 3.1(t, 2H), 2.2(s, 3H), 1.8(m, 1H), 0.9(2s, 6H); IR (KBr Pellets) 2957, 1676, 1480, 1324, 844 cm⁻¹. MS (ES⁺): 497 27q

26q I-2 ¹H NMR (DMSO-d₆): δ 9.06(s, 2H), 8.77(s, 2H), 8.53 (t, J=6Hz, 1H), 8.03(m, 1H), 7.64(m, 6H), 7.46(d, J= 6.9Hz, 1H), 7.05(s, 2H), 6.96(s, 1H), 5.52(s, 1H), 3.02(t, J=6.8Hz, 2H), 1.81(m, 1H), 1.48(s, 6H), 0.85 (d, J=6.8Hz, 6H); MS (ES⁺): 539.4 27r

26r I-2 ¹H NMR (DMSO-d₆): δ 9.06(s, 2H), 8.78(s, 2H), 8.52 (t, J=6Hz, 1H), 8.01(d, J=6.8Hz, 1H), 7.62(m, 7H), 7.46(d, J=6.8Hz, 1H), 7.0(m, 2H), 4.94(t, J=6Hz, 1 H), 3.60(q, J=6 & 12.8Hz, 2H), 3.01(t, J=6Hz, 2H), 2.58(t, J=6Hz, 2H), 1.82(m, 1H), 0.85(d, J=6.8Hz, 6H); MS (ES⁺): 525.4 27s

26s I-2 ¹H NMR (DMSO-d₆): δ 9.01(s, 2H), 8.88(s, 2H), 8.5(t, J=6Hz, 1H), 8.07(m, 1H), 7.73(m, 1H), 7.63(m, 7 H), 7.11(d, J=17Hz, 1H), 7.01(d, J=17Hz, 1H), 6.97 (m, 1H), 6.69(d, J=17Hz, 1H), 5.24(s, 1H), 5.14(s, 1H), 3.03(t, J=6.9 and 6.0Hz, 2H), 1.92(s, 3H), 1.81 (m, 1H), 0.84(d, J=6.9Hz, 6H); MS (ES⁺): 525.4 27t

26t I-2 ¹H NMR (DMSO-d₆): δ 9.08(s, 2H), 8.82(s, 2H), 8.53 (t, J=6Hz, 1H), 8.04(m, 1H), 7.67(m, 7H), 7.04(m, 2 H), 5.55(s, 1H), 5.20(s, 1H), 3.04(t, J=6.9 and 6.0Hz, 2H), 2.19(s, 3H), 1.81(m, 1H), 0.87(d, J=6.9Hz, 6 H); MS (ES⁺): 499.4 27u

26u I-2 ¹H NMR (DMSO-d₆): δ 9.11(s, 2H), 8.86(s, 2H), 8.57 (t, J=6Hz, 1H), 8.13(m, 1H), 7.53(m, 2H), 7.74(m, 6 H), 7.37(d, J=7Hz, 1H), 7.17(m, 2H), 6.54(d, J=12 Hz, 1H), 5.91(m, 1H), 4.99(m, 1H), 4.31(m, 2H), 3.06(t, J=6.9 and 6.0Hz, 2H), 1.83(m, 1H), 0.87(d, J= 6.9Hz, 6H); MS (ES⁺): 515.4 27v

26v I-2 ¹H NMR (DMSO-d₆): δ 9.08(s, 2H), 8.82(s, 2H), 8.54 (t, J=6Hz, 1H), 8.05(m, 1H), 7.63(m, 8H), 7.06(m, 2 H), 5.52(s, 1H), 5.2(s, 1H), 4.63(t, J=5Hz, 1H), 3.56 (m, 2H), 3.05(t, J=6.9 and 6.0Hz, 2H), 2.71(t, J=7 Hz, 2H), 1.82(m, 1H), 0.87(d, J=6.9Hz, 6H); MS (ES⁺): 529.4 27w

26w I-2 ¹H NMR (DMSO-d₆): δ 9.08(s, 2H), 8.86(s, 2H), 8.54 (t, J=6Hz, 1H), 8.03(m, 1H), 7.62(m, 7H), 7.08(d, J= 7.5Hz, 1H), 6.99(m, 1H), 4.32(s, 1H), 3.03(t, J= 6.9 and 6.0Hz, 2H), 2.71(t, J=7Hz, 2H), 1.82(m, 1 H), 0.87(d, J=6.9Hz, 6H); MS (ES⁺): 483.3 27x

26x I-2 ¹H NMR (DMSO-d₆): δ 13.8(s, 1H), 9.04(s, 2H), 8.96 (s, 2H), 8.47(t, J=6Hz, 1H), 7.93(s, 1H), 7.61(m, 6 H), 7.42(m, 1H), 6.91(m, 2H), 6.07(dd, J=17 and 9 Hz, 1H), 5.35(m, 1H), 5.09(dd, J=17 and 11Hz, 1H), 3.38(d, J=6.5Hz, 1H), 3.0(t, J=7Hz, 2H), 1.78(m, 1 H), 1.72(s, 3H), 1.41(s, 3H), 0.84(d, J=6.9Hz, 6H); MS (ES⁺): 527.5 27y

26y I-2 ¹H NMR (DMSO-d₆): δ 8.99(s, 2H), 8.86(s, 2H), 8.52 (t, J=6Hz, 1H), 8.03(m, 1H), 7.63(m, 6H), 7.50(d, J= 7Hz, 1H), 7.07(d, J=7Hz, 1H), 7.12(m, 1H), 5.40 (t, J=6Hz, 1H), 4.33(d, J=6.0Hz, 2H), 3.01(t, J=7 Hz, 2H), 1.80(m, 1H), 0.84(d, J=6.9Hz, 6H); MS (ES⁺): 513.4 27z

26z I-2 ¹H NMR (DMSO-d₆): δ 9.50(bs, 1H), 8.77(bs, 2H), 8.49(t, J=6Hz, 1H), 7.98(m, 1H), 7.63(m, 6H), 7.55 (d, J=6.9Hz, 1H), 7.01(d, J=7.9Hz, 1H), 6.99(m, 1 H), 5.55(s, 1H), 5.38(s, 1H), 5.13(t, J=5Hz, 1H), 4.39(d, J=5Hz, 2H), 3.02(t, J=6.9 and 6.0Hz, 2H), 1.81(m, 1H), 0.86(d, J=6.9Hz, 6H); MS (ES⁺): 515.4 27aa

26aa I-2 ¹H NMR (DMSO-d₆): δ 9.08(s, 2H), 8.73(s, 2H), 8.53 (t, J=6Hz, 1H), 8.06(s, 1H), 8.02(bs, 1H), 7.94(d, J= 7.8Hz, 1H), 7.62(m, 6H), 7.24(d, J=7.8Hz, 1H), 6.95(d, J=7.8Hz, 1H), 3.03(t, J=6Hz, 2H), 1.82(m, 1H), 0.87(d, J=6.8Hz, 6H); MS (ES⁺): 484.3 27ab

26ab I-2 ¹H NMR (DMSO-d₆): δ 9.05(bs, 2H), 8.81(bs, 2H), 8.49(t, J=6Hz, 1H), 8.02(s, 1H), 7.68(s, 1H), 7.62 (m, 6H), 7.53(d, J=6Hz, 1H), 7.21(d, J=6Hz, 1H), 7.13(d, J=7Hz, 1H), 7.01(s, 1H), 5.25(t, J=5Hz, 1 H), 4.51(d, J=5Hz, 2H), 3.01(t, J=6Hz, 2H), 1.81 (m, 1H), 0.85(d, J=6.8Hz, 6H); MS (ES⁺): 571.64 27ac

26ac I-2 ¹H NMR (DMSO-d₆): δ 9.05(bs, 2H), 8.78(s, 2H), 8.52 (t, J=6Hz, 1H), 8.02(bs, 1H), 7.65(m, 6H), 7.53(d, J= 5Hz, 1H), 7.54(d, J=5Hz, 1H), 7.26(d, J=5Hz, 1 H), 7.10(m, 1H), 6.99(m, 1H), 5.64(t, J=5Hz, 1H), 4.71(d, J=5Hz, 2H), 3.07(t, J=6.9 and 6.0Hz, 2H), 1.73(m, 1H), 0.84(d, J=6.9Hz, 6H); MS (ES⁺): 571.56 27ad

26ad I-2 MS (ES⁺): 585.4 27ae

26ae I-2 ¹H NMR (DMSO-d₆): δ 14.11(bs, 1H), 9.05(bs, 2H), 8.75(bs, 2H), 8.5(m, 1H), 8.0(s, 1H), 7.8-7.6(m, 8H), 7.49(d, J=3Hz, 1H), 7.1(d, J=6.9Hz, 1H), 7.0(m, 1 H), 5.5(m, 1H), 4.7(m, 2H), 3.09(m, 2H), 1.74(m, 1 H) 0.86(d, J=6.9Hz, 6H); MS (ES⁺) 571.2 27af

26af I-2 ¹H NMR (DMSO-d₆): δ 14.11(bs, 1H), 9.05(bs, 2H), 8.75(bs, 2H), 8.49(t, J=6Hz, 1H), 7.97(s, 1H), 7.67 (d, J=3Hz, 1H), 7.61(m, 7H), 7.54(d, J=3Hz, 1H), 7.06(d, J=6.9Hz, 1H), 6.89(d, J=6.9Hz, 1H), 5.23 (t, J=5Hz, 1H), 5.42(d, J=5Hz, 2H), 3.09(t, J=6.9 and 6.0Hz, 2H), 1.74(m, 1H) 0.86(d, J=6.9Hz, 6H); MS (ES⁺): 571.3 27ag

26ag I-2 ¹H NMR (DMSO-d₆): δ 11.45(s, 1H), 9.08(bs, 2H), 8.88(bs, 2H), 8.75(t, J=6Hz, 1H), 8.04(bs, 1H), 7.88 (m, 1H), 7.7(m, 7H), 7.03(m, 2H), 6.9(m, 1H), 6.62 (m, 1H), 6.17(m, 1H), 3.07(t, J=6.9 and 6.0Hz, 2H), 1.84(m, 1H), 0.86(d, J=6.9Hz, 6H); MS (ES⁺): 524.65 27ah

26ah I-2 ¹H NMR (DMSO-d₆): δ 13.83(s, 1H), 8.9(bs, 4H), 8.47 (t, J=6Hz, 1H), 7.95(s, 1H), 5.3(s, 1H), 7.61(m, 6 H), 7.4(m, 1H), 6.95(d, J=7.7Hz, 1H), 6.85(d, J=7.7 Hz, 1H), 6.64(d, J=9Hz, 1H), 6.22(s, 1H), 4.6(t, J= 5.1Hz, 1H), 3.51(d, J=5.6Hz, 2H), 3.01(t, J=7Hz, 2H), 1.8(m, 1H), 0.85(d, J=6.9Hz, 6H); MS (ES⁺): 519.52 27ai

26ai I-2 MS (ES⁺) 514.25 27aj

26n G ¹H NMR (DMSO-d₆): δ 9.05(s, 2H), 8.67(s, 2H), 8.47 (t, J=6 and 5Hz, 1H), 7.95(m, 1H), 7.95(m, 1H), 7.63 (m, 5H), 7.40(s, 1H), 7.38(d, J=7.7Hz, 1H), 6.92(m, 2H), 3.02(t, J=6.8Hz, 2H), 2.64(m, 2H), 1.80(m, 1 H), 1.66(m, 2H), 0.96(t, J=8 and 6.5Hz, 3H), 0.85(d, J=6.8Hz, 6H); MS (ES⁻) 499.31 27ak

32f G ¹H NMR (DMSO-d₆): δ 14.3(bs, 1H), 9.05(bs, 2H), 8.75(bs, 2H), 8.5(m, 1H), 8.0(s, 1H), 7.8-7.6(m, 8H), 7.49(d, J=3Hz, 1H), 7.1(d, J=6.9Hz, 1H), 7.0(m, 1 H), 5.5(m, 1H), 4.7(m, 2H), 3.09(m, 2H), 1.74(m, 1 H), 0.86(d, J=6.9Hz, 6H); MS (ES⁺) 487.2 27al

26ai G MS (ES⁺) 488.3 (100%: M⁺¹) 27am

26u G ¹H NMR (DMSO-d₆): δ 13.9(bs, 1H), 9.05(2 bs, 4H), 8.5(m, 1H), 7.9(s, 1H), 7.7-7.5(m, 8H), 7.3(d, J=3 Hz, 1H), 6.9(m, 2H), 4.6(m, 1H), 3.5(m, 2H), 3.09(m, 2H), 2.6(m, 2H), 1.8(m, 1H)0.85(d, J=6.9Hz, 6 H);□ MS (ES⁺) 517.3 32a

31a I-2 ¹H NMR (DMSO-d₆): δ 9.84(bs, 1H), 9.07(bs, 2H), 8.87(bs, 2H), 8.51(t, J=6 and 5Hz, 1H), 8.13(m, 1 H), 8.03(m, 2H), 7.65(m, 5H), 7.20(d, J=7.7Hz, 1 H), 6.94(d, J=7.7.Hz, 1H), 3.04(t, J=6.8Hz, 2H), 2.66(s, 3H), 1.83(m, 1H), 0.86(d, J=6.8Hz, 6H); MS (ES⁻) 499.4, (ES⁺) 501.4 32b

31b I-2 Characterized in the next step 32c

31c I-2 ¹H NMR (DMSO-d₆): δ 14.24(s, 1H), 9.29(bs, 2H), 9.01(bs, 2H), 8.73(t, J=6Hz, 1H), 8.2(d, J=2Hz, 1 H), 7.85(m, 5H), 7.74(d, 2Hz, 1H), 7.4(d, J=8Hz, 1 H), 7.22(d, J=7.4Hz, 1H), 7.13(d, J=7.5, 1H), 6.73 (t, J=6.8Hz, 1H), 5.59(d, J=6.8Hz, 2H), 3.25(t, J= 6.8Hz, 2H), 2.04(m, 1H), 1.08(d, J=6.8Hz, 6H); MS (ES⁻): 495.1, # (ES⁺): 497.2 32d

31d I-2 MS (ES⁻): 553.3 32e

31e I-2 ¹H NMR (DMSO-d₆): δ 13.642(bs, 1H), 9.06(s, 2H), 8.89(s, 2H), 8.50(t, J=6 and 5Hz, 1H), 7.98(s, 1H), 7.62(m, 7H), 7.43(s, 1H), 7.33(m, 4H), 6.95(m, 2H), 4.04(s, 2H), 3.02(t, J=6.8Hz, 2H), 1.80(m, 1H), 0.86(d, J=6.8Hz, 6H); MS (ES⁻): 547.4 32f

31f I-2 ¹H NMR (DMSO-d₆): δ 0.85(d, J=6.9Hz, 6H), 1.81 (m, 1H), 3.03(t, J=7Hz, 2H), 5.35(d, J=11Hz, 1H), 5.94(d, J=17Hz, 1H), 6.84(dd, J=17 and 11Hz, 2H), 7.0(m, 2H), 7.64(m, 8H), 8.01(s, 1H), 8.54(t, J=6 Hz, 1H), 8.77(s, 2H), 9.06(s, 2H); MS (ES⁺): 485.57 32g

31g I-2 MS (ES⁺) 596.2 32h

31h I-2 ¹H NMR (DMSO-d₆): δ 14.2(bs, 1H), 9.1(bs, 4H), 8.6 (m, 1H), 8.15(s, 1H), 7.9-7.6(m, 8H), 7.2(m, 2H), 6.7 (s, 1H), 5.3(br s, 1H), 4.6(m, 2H), 3.1(m, 2H), 1.9(m, 1H), 0.9(d, J=6.7Hz, 6H); MS (ES⁺) 555.1 32i

31i I-2 ¹H NMR (DMSO-d₆): δ 13.84(bs, 1H), 9.01(bs, 2H), 8.80(bs, 2H), 8.46(t, J=6 and 5Hz, 1H), 8.03(s, 1H), 7.95(s, 1H), 7.77(s, 1H), 7.67(m, 2H), 7.61(m, 5H), 7.02(d, J=7.7Hz, 1H), 6.94(m, 1H), 5.13(t, J=5Hz, 1H), 4.47(m, 2H), 2.97(t, J=6.8Hz, 2H), 1.78(m, 1 H), 0.80(d, J=6.8Hz, 6H); MS (ES⁻) 553.3, (ES⁺) 555.3 40

39 I-2 MS (ES⁺) 524.3 44

43 I-2 ¹H NMR (DMSO-d₆): δ 13.82(s, 1H), 9.20(bs, 1H), 9.10(bs, 1H), 8.51(t, J=6Hz, 1H), 7.97(s, 1H), 7.73- 7.45(m, 5H), 7.43-7.39(m, 2H), 7.20(t, J=8Hz, 1H), 7.10(m, 6H), 6.96(d, J=8Hz, 1H), 3.0(t, J=6Hz, 2 H), 1.80(m, 1H), 0.68(d, J=6.8Hz, 6H); MS (ES⁺) 551.30 46

45 I-2 ¹H NMR (DMSO-d₆): δ 9.21(2 bs, 2H each, 4H), 8.61 (m, 1H), 8.1(s, 1H), 7.8-7.4(m, 10H), 7.3(s, 1H), 7.2 (d, J=7Hz, 1H), 7.1(m, 2H), 5.2(s, 2H), 3.1(m, 2H), 1.8(m, 1H), 0.91(d, J=6.8Hz, 6H); MS (ES⁺) 565.27 51 —OCH₃

50 I-2 ¹H NMR (CF₃CO₂D): δ 8.43(s, 1H), 8.01(d, J=7.5Hz, 1H), 7.67(q, J=24 and 8.4Hz, 4H), 7.56(d, J=7.7Hz, 1H), 7.38(s, 1H), 7.23(s, 2H), 3.98(s, 3H), 3.43(d, J= 7Hz, 2H), 2.01(m, 1H), 1.01(d, J=6.8Hz, 6H); MS (ES⁻) 487., (ES⁺) 489.3 53

52 I-2 ¹H NMR (DMSO-d₆): δ 14.00(bs, 1H), 8.52(t, J=6 and 5Hz, 1H), 7.98(s, 1H), 7.63(m, 8H), 7.07(d, J=7.7 Hz, 1H), 6.96(d, J=7.7Hz, 1H), 3.83(s, 2H), 3.02(t, J= 6.8Hz, 2H), 1.81(m, 1H), 0.86(d, J=6.8Hz, 6H); MS (ES⁻) 568.1 70a

68a I-2, S ¹H NMR (DMSO-d₆): δ 13.84(br s, 1H), 9.05(s, 2H), 8.94(s, 2H), 8.48(t, J=5.7Hz, 1H), 7.97(d, J=1.9 Hz, 1H), 7.70(m, 7H), 7.00(d, J=7.9Hz, 1H), 6.92(d, J=7.9Hz, 1H), 6.84(dd, J=10.9 and 17.7Hz, 1H), 5.93(d, J=17.7Hz, 1H), 5.34(d, J=10.9Hz, 1H), 3.19(m, 2H), 1.46(qui, J=7.0Hz, 2H), 1.29(sex, J= 7.0Hz, 2H), 0.87(t, J=7.3Hz, # 3H); MS (ES⁺): 485.2 70b

68b I-2, S ¹H NMR (DMSO-d₆): δ 12.71(br s, 1H), 9.12(s, 2H), 8.93(s, 2H), 8.20(m, 2H), 7.86(m, 1H), 7.70(m, 6H), 7.20(m, 2H), 6.87(dd, J=10.9 and 17.7Hz, 1H), 5.99 (d, J=17.7Hz, 1H), 5.40(d, J=10.9Hz, 1H), 3.97(m, 1H), 1.50-1.20(m, 8H) 0.86(t, J=7.2Hz, 6H); MS (ES⁺): 527.3 70c

68c I-2, S ¹H NMR (DMSO-d₆): δ 12.84(br s, 1H), 9.08(m, 3H), 8.36(d, J=7.7Hz, 1H), 8.18(s, 1H), 7.83(m, 1H), 7.67(m, 6H), 7.15(m, 3H), 6.86(dd, J=10.9 and 17.7 Hz, 1H), 5.98(d, J=17.7Hz, 1H), 5.39(d, J=10.9Hz, 1H), 3.74(m, 1H), 1.84-1.55(m, 5H), 1.38-1.04(m, 5 H); MS (ES⁺): 511.3 70d

68d I-2, S ¹H NMR (DMSO-d₆): δ 9.11(s, 2H), 8.89(s, 2H), 8.81 (t, J=5.7Hz, 1H), 8.21(s, 1H), 7.85(m, 1H), 7.68(m, 7H), 7.17(m, 3H), 6.87(dd, J=10.9 and 17.7Hz, 1H), 5.99(d, J=17.7Hz, 1H), 5.88(m, 1H), 5.39(d, J=10.9 Hz, 1H), 5.12(m, 2H), 3.88(t, J=5.0Hz, 1H); MS (ES⁺): 469.2 70e

68e I-2, S ¹H NMR (DMSO-d₆): δ 9.11(s, 2H), 9.01(s, 2H), 8.38 (d, J=7.5Hz, 1H), 8.18(s, 1H), 7.83(m, 1H), 7.67(m, 6H), 7.16(m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.98(d, J=17.7Hz, 1H), 5.39(d, J=10.9Hz, 1H), 4.09(m, 1H), 1.15(d, J=6.6Hz, 6H); MS (ES⁺): 471.3 70f

68f I-2, S ¹H NMR (DMSO-d₆): δ 9.11(s, 2H), 9.05(s, 2H), 8.31 (d, J=8.1Hz, 1H), 8.20(s, 1H), 7.85(d, J=7.7Hz, 1 H), 7.69(m, 6H), 7.17(m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.98(d, J=17.7Hz, 1H), 5.39(d, J= 10.9Hz, 1H), 3.91(m, 1H), 1.50(m, 2H), 1.12(d, J= 6.6Hz, 3H). 0.85(t, J=7.3Hz, 3H); MS (ES⁺): 485.3 70g

68g I-2, S ¹H NMR (DMSO-d₆): δ 12.82(br s, 1H), 9.25(m, 1H), 9.12(s, 2H), 8.91(s, 2H), 8.23(s, 1H), 7.87(m, 1H), 7.68(m, 7H), 7.18(m, 3H), 6.87(dd, J=10.9 and 17.7 Hz, 1H), 5.99(d, J=17.7Hz, 1H), 5.40(d, J=10.9Hz, 1H), 4.07(m, 2H); MS (ES⁺): 511.2 70h

68h I-2, S ¹H NMR (DMSO-d₆): δ 10.34(s, 1H), 9.05(m, 4H) 8.18 (s, 1H), 7.71(m, 11H), 7.34(t, J=7.8Hz, 2H), 7.09 (m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.98(d, J= 17.7Hz, 1H), 5.39(d, J=10.9Hz, 1H); MS (ES⁺): 505.3 70i

68i I-2, S ¹H NMR (DMSO-d₆): δ 12.64(br s, 1H), 9.09(m, 4H), 8.56(m, 1H), 8.09(s, 1H), 7.66(m, 9H), 7.08(m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.96(d, J=17.7Hz, 1), 5.37(d, J=10.9Hz, 1H), 4.40(m, 2H) 3.39(m, 2 H), 3.22(m, 2H), 1.48(m, 4H); MS (ES⁺): 501.3 (100%: M⁺¹) 70j

68j I-2, S ¹H NMR (DMSO-d₆): δ 9.08(m, 4H), 8.69(t, J=6.0Hz, 1H), 8.16(s, 1H), 7.69(m, 5H), 7.13(d, J=7.7Hz, 2 H), 7.09(m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.97(d, J=17.7Hz, 1H), 5.38(d, J=10.9Hz, 1H), 3.11(t, J=6.0Hz, 2H), 1.01(m, 1H), 0.41(m, 2H), 0.21(m, 2H); MS (ES⁺): 483.3 70k

68k I-2, S ¹H NMR (DMSO-d₆): δ 9.11(s, 2H), 8.97(s, 2H), 8.54 (m, 1H), 8.12(s, 1H), 7.68(m, 7H), 7.17(m, 4H), 6.86 (dd, J=10.9 and 17.7Hz, 1H), 5.97(d, J=17.7Hz, 1 H), 5.38(d, J=10.9Hz, 1H), 2.75(d, J=4.3Hz, 1H); MS (ES⁺): 443.26 70l

68l I-2, S ¹H NMR (DMSO-d₆): δ 9.07(s, 2H), 8.92(s, 2H), 8.53 (t, J=5.5Hz, 1H), 8.02(s, 1H), 7.62(m, 7H), 7.01(m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1H), 5.95(d, J= 17.7Hz, 1H), 5.36(d, J=10.9Hz, 1H), 3.24(qui, J= 6.7Hz, 2H), 1.08(t, J=7.2Hz, 3H); MS (ES⁺): 457.2 70m

68m I-2, S ¹H NMR (DMSO-d₆): δ 12.53(br s, 1H), 9.10(m, 3H), 8.38(d, J=7.9Hz, 1H), 8.11(s, 1H), 7.68(m, 7H), 7.12(m, 3H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.96 (d, J=17.7Hz, 1H), 5.37(d, J=10.9Hz, 1H), 3.94(m, 1H), 1.88-1.33(m, 12H); MS (ES⁺): 525.3 70n

68n I-2, S ¹H NMR (DMSO-d₆): δ 9.09(m, 4H), 8.59(t, J=5.2Hz, 1H), 8.17(s, 1H), 7.70(m, 7H), 7.16(m, 4H), 6.87 (dd, J=10.9 and 17.7Hz, 1H), 5.98(d, J=17.7Hz, 1 H), 5.39(d, J=10.9Hz, 1H), 3.20(q, J=6.7Hz, 2H), 1.52(sex, J=7.2Hz, 2H), 0.87(t, J=7.3Hz, 3H); MS (ES⁺): 471.3 70o

68o I-2, S ¹H NMR (DMSO-d₆): δ 12.97(br s, 1H), 9.08(s, 2H), 8.99(s, 2H), 8.53(t, J=5.1Hz, 1H), 8.06(s, 1H), 7.64 (m, 7H), 7.06(m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1 H), 5.96(d, J=17.7Hz, 1H), 5.36(d, J=10.9Hz, 1H), 3.20(q, J=6.5Hz, 2H), 1.49(qui, J=6.6Hz, 2H), 1.27 (m, 4H), 0.86(t, J=6.6Hz, 3H); MS (ES⁺): 499.3 70p

68p I-2, S ¹H NMR (DMSO-d₆): δ 9.10(s, 2H), 8.91(s, 2H), 8.55 (t, J=5.5Hz, 1H), 8.13(s, 1H), 7.68(m, 7H), 7.12(m, 2H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.98(d, J= 17.7Hz, 1H), 5.38(d, J=10.9Hz, 1H), 3.10(m, 2H), 1.62(m, 1H), 1.39(m, 1H), 1.10(m, 1H), 0.86(m, 6 H); MS (ES⁺): 499.3 70q

68q i-2, s ¹H NMR (DMSO-d₆): δ 9.06(s, 2H), 8.82(s, 2H), 8.11 (t, J=7.9Hz, 1H), 8.00(s, 1H), 7.62(m, 7H), 6.99(m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1H), 5.95(d, J= 17.7Hz, 1H), 5.35(d, J=10.9Hz, 1H), 3.81(q, J=7.5 Hz, 1H), 1.45(m, 4H), 1.24(m, 4H), 0.82(m, 6H); MS (ES⁺): 527.3 70r

68r I-2, S ¹H NMR (DMSO-d₆): δ 13.81(s, 1H), 8.44(m, 4H), 7.97(s, 1H), 7.61(m, 7H), 6.90(m, 3H), 5.93(d, J= 17.7Hz, 1H), 5.34(d, J=10.9Hz, 1H), 3.22(m, 5H), 2.73(m, 2H), 1.52(m, 4H); MS (ES⁺): 500.3 70s

68s I-2, S ¹H NMR (DMSO-d₆): δ 9.09(s, 2H), 8.86(s, 2H), 8.42 (d, J=7.5Hz, 1H), 8.1m1(s, 1H), 7.68(m, 8H), 7.10(m, 2H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.97(d, J= 17.7Hz, 1H), 5.38(d, J=10.9Hz, 1H), 4.20(q, J=7.2 Hz, 1H), 1.93-1.44(m, 8H); MS (ES⁺): 497.2 70t

68t I-2, S ¹H NMR (DMSO-d₆): δ 13.78(br s, 1H), 9.07(s, 2H), 8.87(s, 2H), 8.25(d, J=8.1Hz, 1H), 8.00(s, 1H), 7.62 (m, 7H), 6.98(m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1 H), 5.94(d, J=17.7Hz, 1H), 5.35(d, J=10.9Hz, 1H), 4.55(d, J=4.1Hz, 1H), 3.68(m, 1H), 3.39(m, 1H), 1.79(m, 4H), 1.28(m, 4H); MS (ES⁺): 527.2 70u

68u I-2, S ¹H NMR (DMSO-d₆): δ 13.36(br s, 1H), 9.05(m, 3H), 8.49(s, 1H), 7.98(s, 1H), 7.61(m, 8H), 6.92(m, 3H), 5.94(d, J=17.7Hz, 1H), 5.35(d, J=10.9Hz, 1H), 2.81(m, 1H), 0.69-0.48(m, 4H); MS (ES⁺): 469.3 70v

68v I-2, S ¹H NMR (DMSO-d₆): δ 9.05(m, 4H), 8.75(d, J=7.5 Hz, 1H), 8.15(s, 1H), 7.70(m, 7H), 7.14(d, J=7.9Hz, 2H), 6.86(dd, J=10.9 and 17.7Hz, 1H), 5.97(d, J= 17.7Hz, 1H), 5.39(d, J=10.9Hz, 1H), 4.40(q, J=8.2 Hz, 1H), 2.12(m, 4H) 1.65(m, 2H); MS (ES⁺): 483.3 70w

68w I-2, S ¹H NMR (DMSO-d₆): δ 13.17(br s, 1H), 9.05(m, 4H), 8.51(t,.1=5.8Hz, 1H), 8.06(s, 1H), 7.64(m, 7H), 7.03 (m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1H), 5.95(d, J= 17.7Hz, 1H), 5.36(d, J=10.9Hz, 1H), 4.72(t, J= 5.4Hz, 1H) 3.47(q, J=5.7Hz, 2H), 3.28(m, 2H); MS (ES⁺): 473.2 70x

68x I-2, S ¹H NMR (DMSO-d₆): δ 9.07(s, 2H), 8.90(s, 2H), 8.50 (t, J=5.5Hz, 1H), 8.04(s, 1H), 7.63(m, 7H), 7.03(m, 2H), 6.85(dd, J=10.9 and 17.7Hz, 1H), 5.96(d, J= 17.7Hz, 1H), 5.36(d, J=10.9Hz, 1H), 3.23(q, J=6.5 Hz, 2H), 1.59(m, J=7.0Hz, 1H), 1.39(q, J=6.8Hz, 2 H), 0.88(d, J=6.6Hz, 6H). 70y

68y I-2, S ¹H NMR (DMSO-d₆): δ 13.77(s, 1H), 9.48-8.58(m, 5 H), 7.97(s, 1H), 7.61(m, 6H), 7.03(m, 3H), 6.90(m, 3 H), 5.93(d, J=17.3Hz, 1H), 5.34(d, J=10.5Hz, 1H), 3.22(m, 2H), 2.22(t, J=7.0Hz, 2H), 1.71(t, J=7.3 Hz, 2H); MS (ES⁻): 513.41. 70z

68z I-2, S ¹H NMR (DMSO-d₆-DCl): δ 8.31(s, 1H), 7.98(m, 1H), 7.74(m, 6H), 7.30(m, 2H), 6.88(dd, J=10.5 and 17.3 Hz, 1H), 6.02(d, J=17.3Hz, 1H), 5.41(d, J=10.5Hz, 1H), 3.46(tJ=6.8Hz, 2H), 2.54(m, 2H); MS (ES⁻): 499.32. 70aa

68aa I-2, S ¹H NMR (DMSO-d₆): δ 13.78(s, 1H), 8.68(m, 5H), 8.03(s, 1H), 7.61(m, 7H), 6.89(m, 3H), 5.94(d, J= 17.7Hz, 1H), 5.34(d, J=10.9Hz, 1H), 3.42(m, 2H), 2.93(m, 2H); MS (ES⁺): 472.28. 70ab

68ab I-2, S ¹H NMR (DMSO-d₆): δ 13.41(br s, 1H), 9.10(m, 3H), 8.47(m, 1H), 8.05(s, 1H), 7.65(m, 6H), 7.08-6.78(m, 3H), 6.90(m, 3H), 5.95(d, J=17.3Hz, 1H), 5.36(d, J= 10.5Hz, 1H), 4.82(d, J=5.3Hz, 1H), 4.58(t, J=5.7 Hz, 1H), 3.61(m, 1H), 3.33(m, 2H), 3.18(m, 1H); MS (ES⁺): 503.34. 70ac

68ac I-2, S ¹H NMR (DMSO-d₆): δ 9.02(m, 3H), 8.58(m, 1H), 8.04(s, 1H), 7.72-6.78(m, 12H, 6.90(m, 3H), 5.95(d, J=17.3Hz, 1H), 5.36(d, J=10.5Hz, 1H), 3.40(m, 2 H), 2.32(t, J=7.0Hz, 1H); MS (ES⁺): 500.30.

Cpd. Starting Method No. —R From Used Analytical Data 31a

30a J ¹H NMR(DMSO-d₆): δ10.85(s, 1H), 9.21(s, 2H), 8.91(s, 2H), 8.71(t, J=5.9Hz, 1H), 8.21(d, J=1.96Hz, 1H), 8.23(d, J=1.96Hz, 1H), 8.19(d, J=2.19Hz, 1H), 8.17(d, J=1.97Hz, 1H), 8.09(d, J=1.91Hz, 1H), 7.77(s, 4H), 7.53(d, J=7.53Hz, 1H), 3.57(s, 3H), 3.11(q, J=6.89Hz, 1H), 2.71(s, # 3H), 1.86(m, 1H), 3.88(d, 6.87Hz, 6H); MS(ES+) 515.3 31b

30b J MS(ES⁺): 527.2 31c

30c J Characterized in the next step 31d

30d J ¹HNMR(DMSO-d₆): δ10.59(bs, 1H), 9.16(s, 2H), 8.85(s, 2H), 8.69(t, J=6 and 5Hz, 1H), 8.21(s, 1H), 8.04(d, J=1.5Hz, 1H), 7.73(m, 4H), 7.58(s, 1H), 7.50-7.38(m, 3H), 7.32(m, 1H), 7.03(d, J=7.5Hz, 2H), 4.31(s, 2H), 3.55(s, 2H), 3.07(t, J=6.8Hz, 2H), 1.85(m, 1H), 0.87(d, J=6.8Hz, # 6H),; MS(ES−) 567.3, (ES+) 569.3 31e

30e J MS(ES⁻): 561.4; MS(ES⁺): 563.4 31f

30f J ¹H NMR(DMSO-d₆): δ10.73(s, 1H), 9.24(s, 2H), 9.00(s, 2H), 8.71(t, J=5.7Hz, 1H), 8.24(d, J=1.9Hz, 1H), 8.05(dd, J=8.0, 1.9Hz, 1H), 7.77(m, 5H), 7.71(dd, J=7.9, 1.5Hz, 1H), 7.42(d, J=7.9Hz, 1H), 7.31(d, J=7.9Hz, 1H), 6.89(dd, J=17.6, 11.0Hz, 1H), 6.04(d, J=17.6Hz, 1H), 5.42(d, #J=11.0Hz, 1H), 3.56(s, 3H), 3.10(t, J=6.4Hz, 2H), 1.85(m, 1H), 0.89(d, J=6.7Hz, 6H); MS(ES+): 499.3 31g

30g J ¹H NMR(DMSO-d₆): δ10.73(s, 1H), 9.19(bs, 2H), 8.88(bs, 2H), 8.71(t, J= 6Hz, 1H), 8.27(d, J=2Hz, 1H), 8.07(dd, J=7.7 and 2Hz, 1H), 7.88(d, 2Hz, 1H), 7.8(d, J=2Hz, 1H), 7.83(m, 4H), 7.72(dd, J=2 and 7.7Hz, 1H), 7.46(d, J=7.7, 1H), 7.41(d, J=7.7Hz, 1H), 4.56(s, 2H), 3.56(s, # 3H), 3.11(t, J=6.8Hz, 2H), 1.87(m, 1H), 0.92(d, J=6.8Hz, 6H); MS(ES−) 608.2, (ES+) 610.3 31h

30h J Characterized at the next step 31i

30i J ¹HNMR(DMSO-d₆): δ10.68(s, 1H), 9.17(bs, 2H), 8.82(bs, 2H), 8.68(t, J= 6Hz, 1H), 8.25(d, J=2Hz, 1H), 8.16(d, J=2Hz, 1H), 8.05(dd, J=8 and 2Hz, 1H), 7.87(m, 1H), 7.89(dd, J=8 and 2Hz, 1H), 7.75(m, 5 H), 7.44(d, J=9Hz, 1H), 7.36(d, J=8Hz, 1H), 5.22(t, J=5Hz, 1H), 4.54(d, #J=5Hz, 2H), 3.57(s, 3H), 3.10(t, J=6.8Hz, 2H), 1.84(m, 1H), 0.88(d, J=6.8Hz, 6H; MS(ES−) 567.4, (ES+) 569.4 43

42 J MS(ES⁻): 563.4 45 —Obn 8 J Characterized in the next step 50 —OCH₃ 49 J MS(ES⁺): 503.1 52

31g G Characterized in the next step

No. Starting Method Cpd. —R —R′ From Used Analytical Data 34 —OSO₂CF₃ —H 33 J MS(ES⁺): 621.2 35 —OSO₂CF₃

34 P MS(ES⁺): 755.2; (ES⁻) 753.3 37

35 + 36 D-2 MS(ES⁺): 828.5 38

—H 37 G MS(ES⁺): δ94.4; (E⁻) 692.4 39

—H 38 Q Characterized in the next step

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 54 —OBn —CHO —CO₂MEM 5 + 6 D-2 ¹H NMR(DMSO-d₆): δ9.69(s, 1H), 8.49(d, J=2.0Hz, 1H), 8.22(d, J=6.9Hz, 1H), 7.53(m, 4H), 7.43(m, 2H), 7.37(m, 2H), 7.24(d, J=8.9Hz, 1H), 5.57(s, 2H), 5.26(s, 2H), 3.85(t, J=4.9Hz, 2H), 3.60(s, 3H), 3.51(t, J=4.9Hz 2H), 3.32(s, 3H); MS(ES⁺): 501.02 (M + Na)⁺ 55 —OBn —CO₂H —CO₂MEM 54 E ¹H NMR(DMSO-d₆): δ12.65(s, 1H), 8.41(d, J=2.0Hz 1H), 8.14(dd, J=2.0 and 7.9Hz, 1H), 7.50(m, 3H), 7.38(m, 4H), 7.24(dd, J= 3.0 and 8.9Hz, 1H), 7.11(d, J=8.9Hz, 1H), 5.54(s, 2H), 5.20(s, 2H), 3.82(t, J=4.9Hz, 2H), 3.57(s, 3H), 3.49(t, J=4.9Hz, 2H), 3.23(s, 3H); MS(ES⁻): 493.2 141 —OBn —CHO

140 + 6 D-2 ¹H NMR(DMSO-d₆): δ10.2(s, 1H), 9.65(s, 1H), 8.25(d, J=2.0Hz, 1H), 7.85(dd, J=2.0 and 8.9Hz, 1H), 7.51(d, J=7.9Hz, 2H), 7.45(m, 2H), 7.35(m, 3H), 7.29(d, J= 7.9Hz, 1H) 7.2(d, J=7.9Hz, 1H), 5.24(s, 2H), 3.55(s, 3H), 2.3(d, J=6.9Hz, 2H) 2.1(m, J=6.9Hz, 1H), 1.0(d, J=6.9Hz, 6H); MS(ES⁺): 446.31 142 —OBn —CO₂H

141 E ¹H NMR(DMSO-d₆): δ12.38(s, 1H), 10.01(s, 1H), 8.05(s, 1H), 7.68(d, J=7.9Hz, 1H), 7.41(d, J=7.9Hz, 2H), 7.35(m, 5H), 7.27(m, 1H), 7.11(d, J=8.9Hz, 1H), 7.04(d, J=8.9Hz, 1H), 6.99(d, J=8.9Hz, 1H), 5.11(s, 2H), 2.13(d, J=6.9Hz, 2H), 2.02(m, J=6.9Hz, 1H), 0.852(d, J=6.9Hz, 6H); MS(ES⁻): 460.2 143 —OBn —CO₂MEM

142 F ¹H NMR(DMSO-d₆): δ10.12(s, 1H), 8.16(d, J=1.9Hz, 1H), 7.80(dd, J=1.9 and 8.3Hz, 1H), 7.42(m, 6H), 7.26(dd, J=2.8 and 8.3Hz, 1H), 7.13(m, 2H), 5.21(s, 2H), 5.17(s, 2H), 3.54(s, 3H), 3.40(m, 2H), 3.32(m, 2H), 2.22(d, J=7.0Hz, 2H), 2.10(m, 4H), 0.95(d, J=6.4Hz, 6H); MS(ES⁺): 572.3 (M + Na)⁺ 144 —OH —CO₂MEM

143 G ¹H NMR(DMSO-d₆): δ12.7(br s, 1H), 9.09(s, 2H), 8.91(s, 2H), 8.57(m, 1H), 8.11(s, 1H), 7.92(d, J=1.9Hz, 1H), 7.81(m, 3H), 7.67(m, 5H), 7.14(m, 3H), 6.66(m, 1H), 4.40(t, J=5.3Hz, 1H), 3.39(m, 2H), 3.22(m, 2H), 1.48(m, 4H); MS(ES⁻): 592.2. 145 —OSO₂CF₃ —CO₂MEM

144 B-2 MS(ES⁺): 592.2 146a

—CO₂MEM

145 D-2 MS(ES⁺): 532.5 (M + Na)⁺ 146b

—CO₂MEM

145 D-2 ¹H NMR(DMSO-d₆): δ10.1(s, 1H), 8.21(d, J=2.0Hz, 1H), 8.10(d, J=2.0Hz, 1H), 7.89(dd, J=2.0 and 7.9Hz, 1H), 7.84(d, J=3.0 and 8.9Hz, 1H), 7.63(m, 2H), 7.25(d, J=7.9Hz, 1H), 7.19(m, 2H), 5.22(d, J=14.8Hz, 2H), 3.57(s, 3H), 3.43(t, J=4.9Hz, 2H), 3.34(t, J=4.9Hz, 2H), 3.20(s, 3H), 2.23(d, J=6.9Hz, 2H), # 2.11(m, J= 6.9Hz, 1H), 0.96(d, J=5.9Hz, 6H); MS(ES⁺): 526.48 146c —CH═CH₂ —CO₂MEM

145 D-3 MS(ES⁺): 470.2 (M + Na)⁺ 147a

—CO₂H

146a I-1 MS(ES⁻): 420.29 147b

—CO₂H

146b I-1 ¹H NMR(DMSO-d₆): δ12.65(s, 1H), 10.12(s, 1H), 8.18(d, J=1.9Hz, 1H), 8.07(d, J= 3.0Hz, 1H), 7.83(m, 2H), 7.61(m, 2H), 7.19(m, 3H), 3.56(s, 3H), 2.22(d, J=6.9Hz, 2H), 2.11(m, J=6.9Hz, 1H), 0.96(d, J=6.9Hz, 6H); MS(ES⁺): 438.52 147c —CH═CH₂ —CO₂H

146c I-1 MS(ES⁻): 380.32 173 —H —CHO

172 + 130 D-2 ¹H NMR(DMSO-d₆): δ9.70(s, 1H), 8.42(t, J=6.2Hz, 1H), 7.90(dd, J=1.1 & 6.6Hz, 1H), 7.82(d, J=1.9Hz, 1H), 7.72-7.50(m, 3H), 7.34(d, J=7.7Hz, 1H), 7.27(dd, J=1.3 & 6.2Hz, 1H), 4.38(d, J=6.0Hz, 2H), 3.53(s, 3H), 2.47(m, 1H), 1.07(d, J=7.0Hz, 6H); MS(ES⁺): 340.05 174 —H —CO₂H

173 E ¹H NMR(DMSO-d₆): δ12.35(br s, 1H), 8.31(t, J=7.5Hz, 1H), 7.80-7.31(m, 5H), 7.06(m, 2H), 4.25(d, J=6.0Hz, 2H), 3.41(s, 3H), 2.37(m, 1H), 0.97(d, J=7.0Hz, 6H); MS(ES⁻): 353.83 180 —H —CHO

179 + 130 D-2 ¹H NMR(DMSO-d₆): δ9.70(s, 1H), 7.87(m, 2H), 7.69(m, 1H), 7.55(m, 2H), 7.35(d, J= 7.9Hz, 1H), 7.27(d, J=7.5Hz, 1H), 4.51(s, 2H), 3.52(s, 3H), 3.05(m, 2H), 1.92(m, 1H), 1.40(m, 9H), 0.85(d, J =6.8Hz, 6H); MS(ES⁺): 448.3 (M + Na)⁺ 181 —H —CO₂H

180 E ¹H NMR(DMSO-d₆): δ7.81(m, 2H), 7.56(m, 1H), 7.44(m, 2H), 7.16(m, 2H), 4.47(s, 2H), 3.51(s, 3H), 3.02(m, 2H), 1.92(m, J=7.0Hz, 1H), 1.41(m, 9H), 0.85(d, J=6Hz, 6H); MS(ES⁻): 440.2 184a —OBn —CHO

3a + 6 D-2 ¹H NMR(DMSO-d₆): δ□9.78(s, 1H), 8.85(t, J=5.7Hz, 1H), 8.50(d, J=2.0Hz, 1H), 8.20(dd, J=8.2, 1.9Hz, 1H), 7.55(m, 9H), 5.35(s, 2H), 3.69(s, 3H), 3.23(t, J=6.5Hz, 2H), 1.98(m, 1H), 1.02(d, J=6.8Hz, 6H); MS(ES⁺): 446.3 184b —OBn —CHO

3f + 6 D-2 MS(ES⁻): 470.2 184c —OBn —CHO

3i + 6 D-2 MS(ES⁻): 418.3 184d —OBn —CHO

3j + 6 D-2 MS(ES⁺): 460.3 185a —OH —CHO

184a AD ¹H NMR(DMSO-d₆): δ10.06(s, 1H), 9.63(s, 1H), 8.73(t, J=6.5Hz, 1H), 8.36(d, J=2Hz, 1H), 8.09(dd, J=2 and 8Hz, 1H), 7.45(d, J=8Hz, 1H), 7.28(s, 1H), 7.11(s, 2H), 3.58(s, 3H), 3.13(d, J=7Hz, 2H), 1.87(m, 1H), 0.91(d, J=6.8Hz, 6H); MS(ES−): 354.2 and (ES⁺) 378.2 (M + Na)⁺) 185b —OH —CHO

184b AD MS(ES⁻): 380.1 185c —OH —CHO

184c AD ¹HNMR(DMSO-d₆): δ10.21(s, 1H), 9.78(s, 1H), 8.87(t, J=5.80Hz, 1H), 8.51(s, 1H), 8.23(d, J=7.92Hz, 1H), 7.60(d, J=7.9Hz, 1H), 7.43(s, 1H), 7.25(s, 2H), 3.74(s, 3H), 3.46(q, J=5.65, 2H), 1.32(t, J=7.8Hz, 3H) 185d —OH —CHO

184d AD ¹HNMR(DMSO-d₆): δ10.06(s, 1H), 9.62(s, 1H), 8.69(t, J=5.90Hz, 1H), 8.36(s, 1H), 8.08(d, J=7.92Hz, 1H), 7.45(d, J=8.1Hz, 1H), 7.28(s, 1H), 7.10(s, 2H), 3.58(s, 3H), 3.22(m, 1H), 3.11(m, 1H), 1.66(m, 1H), 1.44(m, 1H), 1.18(m, 1H), 0.89(t, J=6.4Hz, 6H). 186a —OSO₂CF₃ —CHO

185a B-2 MS(ES⁺): 488.24 186b —OSO₂CF₃ —CHO

185b B-2 ¹HNMR(DMSO-d₆): δ9.74(s, 1H), 9.44(t, J= 5.90Hz, 1H), 8.51(s, 1H), 8.11(d,J =7.91Hz, 1H), 7.54(m, 4H), 4.18(m, 2H), 3.59(s, 3H). 186c —OSO₂CF₃ —CHO

185c B-2 ¹HNMR(DMSO-d₆): δ9.45(s, 1H), 8.59(t, J=5.90Hz, 1H), 8.28(s, 1H), 7.94(d, J=8.10Hz, 1H), 7.79(d, J=2.8Hz, 1H), 7.67(d, J=7.9Hz, 1H), 7.32(d, J=7.9Hz, 2H), 3.40(s, 3H), 3.12(q, J=7.1Hz, 2H), 0.97(t, J=7.16Hz, 3H). 186d —OSO₂CF₃ —CHO

185d B-2 ¹HNMR(DMSO-d₆): δ9.71(s, 1H), 8.78(t, J=5.90Hz, 1H), 8.49(s, 1H), 8.18(d, J=7.92Hz, 1H), 8.00(s, 1H), 7.88(d, J=8.5 1Hz, 1H), 7.52(q, J=8.1Hz, 2H), 3.67(s, 3H), 3.22(m, 1H), 3.16(m, 1H), 1.68(m, 1H), 1.44(m, 1H), 1.18(m, 1H), 0.89(t, J=6.4Hz, 6H). 187a —CH═CH₂ —CHO

186a D-3 ¹HNMR(DMSO-d₆): δ9.74(s, 1H), 8.76(t, J=6.5Hz, 1H), 8.42(d, J=2Hz, 1H), 8.11(dd, J=2 and 8Hz, 1H), 8.00(d, J=1.7Hz, 1H), 7.84(dd, J=8 and 2Hz, 1H), 7.47(d, J= 8Hz, 1H), 7.27(d, J=8Hz, 1H), 6.90(dd, J=11 and 17.7Hz, 1H), 6.01(d, J=17.7Hz, 1H), 5.42(d, # J=11Hz, 1H), 3.59(s, 3H), 3.14(d, J=7Hz, 2H), 1.88(m, 1H), 0.92(d, J=6.8Hz, 6H); MS(ES−): 364.2 and (ES⁺) 388.2 (M + Na)⁺ 187b —CH═CH₂ —CHO

186b D-3 MS(ES⁻): 390.1 187c —CH═CH₂ —CHO

186c D-3 MS(ES⁻): 336.2 187d —CH═CH₂ —CHO

186d D-3 MS(ES⁻): 378.2

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 56 —OBn —H —CO₂MEM 55 J ¹H NMR(DMSO-d₆): δ10.67(s, 1H), 9.2(s, 2H), 8.87(s, 2H), 8.33(d, J=2.0Hz, 1H), 8.17(dd, J=2.0 and 7.9Hz, 1H), 7.77(s, 4H), 7.49(m, 4H), 7.39(m, 2H), 7.30(s, 2H), 5.54(s, 2H), 5.27(s, 2H), 3.83(t, J= 4.9Hz, 2H), 3.57(s, 3H), 3.49(t, J=4.9Hz, 2H), 3.23(s, 3H); MS(ES⁺): 612.4 57 —OBn —Boc —CO₂MEM 56 R MS(ES⁺): 712.4 58 —OH —Boc —CO₂MEM 57 G ¹H NMR(DMSO-d₆): δ10.4(s, 1H), 10.0(s, 1H), 8.9(s, 1H), 8.28(d, J=2.0Hz, 1H), 8.12(dd, J=2.1 and 7.7Hz, 1H), 7.89(d, J=8.4Hz, 2H), 7.61(d, J= 8.4Hz, 2H), 7.45(d, J=7.7Hz, 1H), 7.13(d, J=8.4Hz, 1H), 7.06(s, 1H), 6.98(dd, J=2.8 and 8.4Hz, 1H), 5.52(s, 2H), 3.81(t, J=4.9Hz, 2H), 3.56(s, 3H), 3.46(t, J=4.9Hz, 2H), 3.20(s, 3H), 1.43(s, 9H); MS(ES⁻): 620.5 59 —OSO₂CF₃ —Boc —CO₂MEM 58 B-2 ¹H NMR(DMSO-d₆): δ10.55(s, 1H), 8.38(d, J=2.0Hz, 1H), 8.18(dd, J=2.0 and 7.9Hz, 1H), 7.86(m, 4H), 7.75(dd, J=2.0 and 8.9Hz, 1H), 7.54(m, 5H), 5.51(s, 2H), 3.77(t, J=4.9Hz, 2H), 3.55(s, 3H), 3.46(t, J=4.9Hz, 2H), 3.18(s, 3H) 1.41(s, 9H); MS(ES⁺): 754.3 60

—Boc —CO₂MEM 59 D-2 ¹H NMR(DMSO-d₆): δ10.61(s, 1H), 8.94(s, 1H), 8.37(s, 1H), 8.19(dd, J=2.0 and 7.9Hz, 1H), 8.02(s, 1H), 7.89(m, 5H), 7.65(d, J=8.9Hz, 2H), 7.54(d, J=7.9Hz, 1H), 7.39(d, J=7.9Hz, 1H), 7.17(d, J=3.9Hz, 1H), 6.68(m, 1H), 5.54(s, 2H), 3.82(t, J=4.9Hz, 2H), 3.58(s, 3H), 3.49(t, J= #4.9Hz, 2H), 3.22(s, 3H), 1.45(s, 9H); MS(ES⁺): 672.5 61

—Boc —CO₂H 60 I-1 ¹H NMR(DMSO-d₆): δ10.50(s, 1H), 8.96(s, 1H), 8.32(s, 1H), 8.07(d, J=7.9Hz, 1H), 7.98(s, 1H), 7.87(m, 5H), 7.63(d, J=8.9Hz, 2H), 7.38(m, 2H), 7.15(d, J=3.0Hz, 1H), 6.67(m, 1H), 3.57(s, 3H), 1.45(s, 9H); MS(ES¹): 582.4 66 —CH═CH₂ —Boc —CO₂MEM 59 D-3 ¹H NMR(DMSO-d₆): δ10.56(s, 1H), 9.02(br s, 1H), 8.35(d, J=1.7Hz, 1H), 8.18(dd, J=1.9 and 6.0Hz, 1H), 7.88(d, J=9.0Hz, 2H), 7.80(d, J=1.3Hz, 1H), 7.71(dd, J=1.7 and 6.2Hz, 1H), 7.63(d, J=8.9Hz, 2H), 7.50(d, J=8.3Hz, 1H), 7.32(d, J=8.1Hz, 1H), 6.89(dd, J=10.7 and 17.7Hz, 1H), 6.04(d, J=17.4Hz, 1H), 5.54(s, 2H), 5.43(d, J=11.7Hz, 1H), 3.82(t, J=4.5Hz, 2H), 3.57(s, 3H), 3.48(t, J=4.5Hz, 2H), 3.22(s, 3H), 1.44(s, 9H); MS(ES⁺): 632.1 67 —CH═CH₂ —Boc —CO₂H 66 I-1 ¹H NMR(DMSO-d₆): δ10.49(s, 1H), 8.99(br s, 1H), 8.31(s, 1H), 8.07(d, J=8.3Hz, 1H), 7.87(d, J=9.0Hz, 2H), 7.77(m, 2H), 7.66(m, 3H), 7.38(d, J=7.7Hz, 1H), 7.29(d, J=7.7Hz, 1H), 6.88(dd, J=10.7 and 17.7Hz, 1H), 6.03(d, J=17.4Hz, 1H), 5.41(d, J= 10.9Hz, 1H), 3.56(s, 3H), 1.43(s, 9H); MS(ES⁻): 542.1

Cpd. Starting Method No. —R —R′ From Used Analytical Data 62a —CH₃

61 A-4 ¹H NMR(DMSO-d₆): δ10.57(s, 1H), 8.92(s, 1H), 8.64(t, J=5.4Hz, 1H), 8.24(d, J=2.0Hz, 1H), 8.02(dd, J=2.0 and 7.9Hz, 1H), 7.98(s, 1H), 7.88(m, 3H) 7.84(s, 1H), 7.64(d, J=8.9Hz, 2H), 7.42(d, J=7.9Hz, 1H), 7.36(d, J=7.9Hz, 1H), 7.14(d, J=3.0Hz, 1H), 6.67(m, 1H), 3.55(s, 3H), 3.26(m, 2H), 1.50(m, # J=7.4Hz, 2H), 1.43(s, 9H), 1.32(m, J=7.4Hz, 2H), 0.89(t, 3H); MS(ES⁻): 639.5 62b —CH₃

61 A-4 MS(ES⁺): 625.5 62c —CH₃

61 A-4 MS(ES⁺): 623.4 62d —CH₃

61 A-4 MS(ES⁺): 687.4 62e —CH₃

61 A-4 MS(ES⁺): 625.4 62f —CH₃

61 A-4 MS(ES⁺): 653.5 62g —CH₃

61 A-4 MS(ES⁺): 653.5 62h —CH₃

61 A-4 MS(ES⁺): 667.3 62i —CH₃

61 A-4 MS(ES⁺): 681.5 62j —CH₃

61 A-4 MS(ES⁺): 637.3 62k —CH₃

61 A-4 MS(ES⁺): 640.3 62l —CH₃

61 A-4 MS(ES⁺): 665.4 62m —CH₃

61 A-4 MS(ES⁺): 597.3 62n —CH₃

61 A-4 MS(ES⁺): 639.4 62o —CH₃

61 A-4 MS(ES⁺): 695.4(M + Na)⁺ 62p —CH₃

61 A-4 MS(ES⁻): 665.4 62q —CH₃

61 A-4 MS(ES⁺): 653.4 62r —CH₃

61 A-4 MS(ES⁺): 567.3 62s —CH₃

61 A-4 MS(ES⁺): 667.5 62t —CH₃

61 A-4 MS(ES⁺): 641.3 62u —CH₃

61 A-4 MS(ES⁺): 655.3 62v —CH₃

61 A-4 MS(ES⁺): 663.1 62w —CH₃

61 A-4 MS(ES⁻): 577.2 62x —CH₃

61 A-4 MS(ES⁺): 679.2 62y —CH₃

61 A-4 MS(ES⁺): 621.1 62z —CH₃

61 A-4 MS(ES⁺): 611.1 62aa —CH₃

61 A-4 MS(ES⁺): 657.1 62ab —CH₃

61 A-4 MS(ES⁺): 659.1 62ac —CH₃

61 A-4 MS(ES⁺): 679.3 62ad —CH₃

61 A-4 MS(ES⁻): 695.3 62ae —CH₃

61 A-4 MS(ES⁺): 651.3 62af —CH₃

61 A-4 MS(ES⁺): 679.4 62ag —CH₃

61 A-4 MS(ES⁻): 667.32

Cpd. Starting Method No. —R —R′ From Used Analytical Data 64a

62a I-2, S ¹H NMR (DMSO-d₆): δ 12.80 (s, 1H), 9.09 (s, 2H), 8.91 (s, 2H), 8.57 (m, 1H), 8.15 (s, 1H), 7.91 (s, 1H), 7.80 (m, 3H), 7.67 (m, 4H), 7.20 (m, 2H), 7.07 (s, 1H), 6.63 (s, 1H) 3.21 (m, J=5.9Hz, 2H), 1.46 (m, J=7.4Hz, 2H), 1.28 (m, J=7.4Hz, 2H) 0.86 (t, J=7.4Hz, 3H); MS (ES⁺): 525.3 64b

62b I-2, S ¹H NMR (DMSO-d₆): δ 12.76 (s, 1H), 9.10 (s, 2H), 8.82 (s, 2H), 8.59 (m, 1H), 8.20 (s, 1H), 7.95 (s, 1H), 7.83 (m, 3H), 7.70 (s, 4H), 7.25 (m, 2H), 7.10 (s, 1H), 6.65 (s, 1H), 3.20 (q, J=6.0Hz, 2H), 1.51 (m, J=7.4Hz, 2H), 0.87 (t, J=7.4Hz, 3H); MS (ES⁺): 511.2 64c

62c I-2, S ¹H NMR (DMSO-d₆): δ 12.84 (s, 1H), 9.11 (s, 2H), 8.84 (m, 2H), 8.26 (m, 1H), 7.94 (m, 2H), 7.83 (m, 3H), 7.71 (s, 4H), 7.28 (m, 2H), 7.12 (s, 1H), 6.65 (s, 1H), 5.87 (m, 1H), 5.15 (d, J=17.2Hz, 1H), 5.07 (d, J= 10.3Hz, 1H) 3.88 (t, J=5.2Hz, 2H); MS (ES⁺): 509.2 64d

62d I-2, S ¹H NMR (DMSO-d₆): δ 12.78 (s, 1H), 9.11 (m, 2H), 8.85 (s, 2H), 8.22 (s, 1H), 7.93 (s, 1H), 7.83 (m, 3H), 7.68 (s, 4H), 7.19 (m, 3H), 7.10 (m, 5H), 6.65 (s, 1H), 4.41 (s, 2H), 2.27 (s, 3H); MS (ES⁺): 573.3 64e

62e I-2, S ¹H NMR (DMSO-d₆): δ 12.82 (s, 1H), 9.11 (s, 2H), 8.86 (s, 2H), 8.39 (d, J=7.7Hz, 1H), 8.24 (s, 1H), 7.95 (s, 1H), 7.90 (m, 1H), 7.84 (m, 2H), 7.71 (s, 4H), 7.28 (m, 2H), 7.11 (m, 1H), 6.65 (s, 1H), 4.08 (m, J=6.9Hz, 1H), 1.14 (d, J=6.9Hz, 6H); MS (ES⁺): 511.3 64f

62f I-2, S ¹H NMR (DMSO-d₆): δ 13.28 (br s, 1H), 9.05 (m, 2H), 8.84 (s, 2H), 8.46 (m, 1H), 7.99 (s, 1H), 7.88 (s, 1H), 7.77 (m, 2H), 7.63 (m, 5H), 7.07 (m, 2H), 6.96 (m, 1H), 6.63 (s, 1H), 3.16-2.96 (m, 2H), 1.65-1.03 (m, 3H), 0.85 (m, 6H); MS (ES⁺): 539.3 64g

62g I-2, S ¹H NMR (DMSO-d₆): δ 13.37 (s, 1H), 9.06 (s, 2H), 8.84 (s, 2H), 8.47 (m, 1H), 8.00 (s, 1H), 7.88 (s, 1H), 7.78 (m, 2H), 7.70 (m, 5H), 7.08 (m, 2H), 6.97 (s, 1H), 6.63 (s, 1H), 3.22 (m, 2H), 1.58 (m, J=6.0Hz, 1H), 1.38 (m, J=6.9Hz, 2H), 0.87 (d, J=6.9Hz, 6H); MS (ES⁺): 539.3 64h

62h I-2, S ¹H NMR (DMSO-d₆): δ 12.71 (br s, 1H), 9.13 (s, 1H), 8.75 (m, 3H), 8.31 (m, 1H), 7.97 (m, 2H), 7.86 (m, 2H), 7.73 (m, 4H), 7.64 (m, 2H), 7.33 (m, 2H), 7.13 (m, 1H), 6.67 (m, 1H), 3.98 (m, 1H), 3.77 (q, J=6.9Hz, 1H), 3.62 (q, J=6.9Hz, 1H), 3.29 (m, 2H), 1.86 (m, 3H), 1.59 (m, 1H); MS (ES⁺): 553.3 64i

62i I-2, S ¹H NMR (DMSO-d₆): δ 12.81 (br s, 1H), 9.13 (s, 2H), 8.85 (s, 2H), 8.26 (m, 2H), 7.96 (m, 2H), 7.86 (m, 2H), 7.74 (m, 5H), 7.32 (m, 1H), 7.13 (m, 1H), 6.67 (m, 1H), 3.99 (m, 1H), 1.5-0.85 (m, 14H); MS (ES⁺): 567.3 64j

62j I-2, S ¹H NMR (DMSO-d₆): δ 13.74 (br s, 1H), 9.07 (s, 2H), 8.92 (s, 2H), 8.62 (t, J=5.6Hz, 1H), 8.03 (s, 1H), 7.89 (d, J=1.7Hz, 1H), 7.79 (m, 2H), 7.64 (m, 4H), 7.10 (m, 3H), 6.99 (d, J=8.5Hz, 1H), 6.64 (m, 1H), 3.08 (t, J= 6.0Hz, 2H), 1.00 (m, 1H), 0.40 (m, 2H), 0.20 (m, 2H); MS (ES⁺): 523.4 64k

62k I-2, S ¹H NMR (DMSO-d₆): δ 9.12 (s, 2H), 8.88 (s, 2H), 8.52 (m, 1H), 8.12 (m, 1H), 7.92 (m, 2H), 7.81 (m, 3H), 7.67 (m, 4H), 7.14 (m, 3H), 6.66 (m, 1H), 4.75 (d, J=4.5Hz, 1H), 3.77 (m, 1H), 3.17 (m, 1H), 1.04 (d, J= 6.0Hz, 3H); MS (ES⁺): 527.2 64l

62l I-2, S ¹H NMR (DMSO-d₆): δ 13.91 (br s, 1H), 9.07 (s, 2H), 8.90 (s, 2H), 8.29 (d, J=8.1Hz, 1H), 8.00 (s, 1H), 7.89 (m, 1H), 7.78 (m, 2H), 7.64 (m, 5H), 7.08 (m, 2H), 6.96 (d, J=7.7Hz 1H), 6.64 (m, 1H), 3.71 (m, 1H), 1.82- 1.03 (m, 10H)p; MS (ES⁺): 551.33 64m

62m I-2, S ¹H NMR (DMSO-d₆): δ 13.87 (br s, 1H), 9.07 (s, 2H), 8.90 (s, 2H), 8.48 (m, 1H), 7.99 (s, 1H), 7.89 (m, 1H), 7.79 (m, 2H), 7.62 (m, 5H), 7.10 (m, 2H), 6.97 (d, J=7.9Hz 1H), 6.64 (m, 1H), 2.73 (d, J=4.5Hz, 3H); MS (ES⁺): 483.2 64n

62n I-2, S ¹H NMR (DMSO-d₆): δ 9.08 (s, 2H), 8.85 (s, 2H), 8.26 (d, J=8.7Hz, 1H), 8.07 (s, 1H), 7.91 (s, 1H), 7.80 (m, 2H), 7.67 (m, 5H), 7.09 (m, 3H), 6.65 (m, 1H), 3.89 (m, J=7.0Hz, 1H), 1.49 (m, J=6.9Hz, 2H), 1.10 (d, J= 6.6Hz, 3H), 0.85 (t, J=7.2Hz, 3H); MS (ES⁺): 525.2 64o

62o I-2, S ¹H NMR (DMSO-d₆): δ 9.19 (m, 2H), 9.10 (s, 2H), 8.82 (s, 2H), 8.19 (m, 1H), 7.94 (s, 1H), 7.83 (m, 2H), 7.68 (m, 4H), 7.33-7.10 (m, 8H), 6.66 (m, 1H), 4.45 (d, J=5.7Hz, 2Hz); MS (ES⁺): 559.2 64p

62p I-2, S ¹H NMR (DMSO-d₆): δ 9.22 (m, 2H), 9.09 (s, 2H), 8.81 (s, 2H), 8.17 (m, 1H), 7.95 (s, 1H), 7.82 (m, 2H), 7.68 (m, 4H), 7.16 (m, 4H), 6.66 (m, 1H), 4.06 (m, 2H); MS (ES⁺): 551.22 64q

62q I-2, S ¹H NMR (DMSO-d₆): δ 9.10 (s, 2H), 8.86 (s, 2H), 8.56 (m, 1H), 8.13 (m, 1H), 7.93 (s, 1H), 7.82 (m, 2H), 7.67 (m, 5H), 7.15 (m, 3H), 6.66 (m, 1H), 3.19 (m, 2H), 1.50 (m, 2H), 1.28 (m, 4H), 0.87 (t, J=7.0Hz, 3H); MS (ES⁺): 539.3 64r

62r I-2, S ¹H NMR (DMSO-d₆): δ 9.09 (s, 2H), 8.90 (m, 2H), 8.15 (m, 2H), 7.93 (s, 1H), 7.81 (m, 3H), 7.68 (m, 4H), 7.13 (m, 3H), 6.66 (m, 1H), 3.83 (m, 1H), 1.47 (m, 4H), 1.25 (m, 4H), 0.83 (m, 6H); MS (ES⁺): 567.3 64s

62s I-2, S ¹H NMR (DMSO-d₆): δ 9.08 (s, 2H), 8.86 (s, 2H), 8.48 (m, 1H), 8.03 (m, 1H), 7.90 (s, 1H), 7.79 (m, 2H), 7.65 (m, 5H), 7.12 (m, 2H), 7.02 (m, 1H), 6.65 (m, 1H), 3.22 (m, 2H), 1.42 (t, J=8.2Hz, 2H), 0.91 (s, 9H); MS (ES⁺): 553.4 64t

62t I-2, S ¹H NMR (DMSO-d₆): δ 13.61 (br s, 1H), 9.07 (s, 2H), 9.00 (s, 2H), 8.52 (t, J=5.5Hz, 1H), 8.02 (s, 1H), 7.90 (d, J=1.9Hz, 1H), 7.79 (m, 2H), 7.64 (m, 5H), 7.10 (m, 2H), 7.00 (d, J=7.7Hz, 1H), 6.64 (m, 1H), 4.47 (t, J= 5.3Hz, 1H), 3.43 (m, 2H), 3.27 (m, 2H), 1.64 (qui, J=6.8Hz, 2H); MS (ES⁺): 527.23 64u

62u I-2, S ¹H NMR (DMSO-d₆): δ 12.7 (br s, 1H), 9.09 (s, 2H), 8.91 (s, 2H), 8.57 (m, 1H), 8.11 (s, 1H), 7.92 (d, J=1.9Hz, 1H), 7.81 (m, 3H), 7.67 (m, 5H), 7.14 (m, 2H), 6.66 (m, 1H), 4.40 (t, J=5.3Hz, 1H), 3.39 (m, 2H), 3.22 (m, 2H), 1.48 (m, 4H); MS (ES⁺): 541.34 64v

62v I-2, S ¹H NMR (DMSO-d₆): δ 9.16-8.89 (m, 4H), 8.16 (m, 1H), 7.93 (s, 1H), 7.81 (m, 3H), 7.67 (m, 4H), 7.56 (s, 1H), 7.15 (m, 5H), 6.65 (m, 1H), 6.38 (m, 1H), 6.26 (m, 1H), 4.42 (d, J=4.9Hz, 2H); MS (ES⁺): 549.27 64w

62w I-2, S ¹H NMR (DMSO-d₆): δ 11.59 (br s, 1H), 9.14 (s, 2H), 8.98 (s, 2H), 8.70 (t, J=5.7Hz, 1H), 8.24 (s, 1H), 7.99 (m, 2H), 7.87 (m, 3H), 7.71 (m, 3H), 7.36 (s, 1H), 7.27 (m, 2H), 7.10 (m, 2H), 6.67 (m, 1H), 4.07 (t, J=6.9Hz, 2H), 3.24 (q, J=6.5Hz, 2H), 1.98 (qui, J=6.7Hz, 2H); MS (ES⁺): 577.17 64x

62x I-2, S ¹H NMR (DMSO-d₆): δ 13.72 (br s, 1H), 9.13 (s, 2H), 9.06 (s, 2H), 8.50 (t, J=5.7Hz, 1H), 8.00 (d, J=1.3Hz, 1H), 7.89 (d, J=1.9Hz, 1H), 7.78 (m, 2H), 7.62 (m, 4H), 7.08 (m, 2H), 6.96 (d, J=7.9Hz, 1H), 6.64 (m, 1H), 3.04 (t, J=6.5Hz, 2H), 1.72-1.43 (m, 6H), 1.25-1.08 (m, 3H), 0.88 (m, 2H); MS (ES⁺): 565.25 64y

62y I-2, S ¹H NMR (DMSO-d₆): δ 9.16-8.87 (m, 4H), 8.09 (s, 1H), 7.91 (s, 1H), 7.80 (m, 2H), 7.65 (m, 5H), 7.12 (m, 5H), 6.65 (m, 1H), 4.01 (m, 2H), 3.10 (m, 1H); MS (ES⁺): 507.2 64z

62z I-2, S ¹H NMR (DMSO-d₆): δ 9.10 (s, 2H), 8.97 (s, 2H), 8.59 (t, J=5.7Hz, 1H), 8.13 (s, 1H), 7.93 (s, 1H), 7.80 (m, 3H), 7.68 (m, 4H), 7.16 (m, 4H), 6.65 (m, 1H), 3.26 (qui, J=6.0Hz, 2H), 1.10 (t, J=7.2Hz, 3H); MS (ES⁺): 497.2 64aa

62aa I-2, S ¹H NMR (DMSO-d₆): δ 14.1 (br s, 1H), 9.08 (s, 2H), 8.79 (s, 2H), 8.45 (m, 1H), 8.01 (s, 1H), 7.90 (s, 1H), 7.79 (m, 3H), 7.63 (m, 5H), 7.09 (m, 2H), 6.98 (m, 1H), 6.65 (m, 1H), 4.80 (d, J=4.7Hz, 1H), 4.56 (t, J= 6.8Hz, 1H), 3.60 (m, 1H), 3.32-2.90 (m, 3H); MS (ES⁺): 543.2 64ab

62ab I-2, S ¹H NMR (DMSO-d₆): δ 10.34 (s, 1H), 9.07 (s, 2H), 8.85 (s, 2H), 8.18 (s, 1H), 7.93 (s, 1H), 7.80 (m, 6H), 7.66 (m, 4H), 7.34 (m, 2H), 7.11 (m, 4H), 6.65 (m, 1H); MS (ES⁺): 545.2 64ac

62ac I-2, S ¹H NMR (DMSO-d₆): δ 9.07 (m, 4H), 8.38 (d, J=8.5Hz, 1H), 8.10 (s, 1H), 7.92 (s, 1H), 7.84-7.62 (m, 7H), 7.11 (m, 3H), 6.66 (m, 1H), 3.94 (m, 1H), 1.88-1.35 (m, 12H); MS (ES⁺): 565.3 64ad

62ad I-2, S ¹H NMR (DMSO-d₆): δ 13.71 (m, 2H), 9.36-8.57 (m, 4H), 8.50 (m, 1H), 7.98 (s, 1H), 7.89 (s, 1H), 7.78 (2H), 7.61 (m, 5H), 7.08 (m, 2H), 6.95 (d, J=7.9Hz, 1H), 6.63 (m, 1H), 3.19 (m, 2H), 2.16 (t, J=7.2Hz, 2H), 1.48 (m, 4H), 1.28 (m, 2H); MS (ES⁻): 581.2 64ae

64ae I-2, S ¹H NMR (DMSO-d₆): δ 9.12 (s, 2H), 8.89 (s, 2H), 7.91 (m, 1H), 7.81 (m, 2H), 7.70 (d, J=8.7Hz, 2H), 7.62 (d, J=8.9Hz, 2H), 7.48 (m, 1H), 7.22 (m, 2H), 7.11 (d, J=3.4Hz, 1H), 7.05 (d, J=7.2Hz, 1H), 6.65 (m, 1H), 3.53 (m, 2H), 3.08 (m, 2H), 1.62-1.21 (m, 6H); MS (ES⁺): 537.20 64af

64af I-2, S ¹H NMR (DMSO-d₆): δ 12.81 (br s, 1H), 9.13 (s, 2H), 8.82 (s, 2H), 7.95 (s, 1H), 7.85 (m, 2H), 7.71 (m, 5H), 7.43 (m, 1H), 7.29 (m, 2H), 7.13 (m, 1H), 6.67 (m, 1H), 3.49-2.97 (m, 4H), 1.67-1.37 (m, 2H), 1.08 (m, 1H), 0.90 (m, 3H), 0.61-0.26 (m, 4H); MS (ES⁺): 565.3 64ag

62ag I-2, S ¹H NMR (DMSO-d₆): δ 13.78 (s, 1H), 9.09-8.22 (m, 5H), 7.97 (s, 1H), 7.89 (s, 1H), 7.77 (m, 2H), 7.61 (m, 5H), 7.03 (m, 3H), 6.64 (m, 1H), 3.22 (m, 2H), 2.20 (t, J=7.0Hz, 2H), 1.71 (t, J=7.3Hz, 2H); MS (ES⁻): 553.24.

Cpd. Starting Method No. —R —R′ From Used Analytical Data 65

61 A-4, I-2, S ¹H NMR (DMSO-d₆, D₂O): δ 13.87 (br s, 1H), 9.56 (m, 2H) 9.21 (s, 1H), 8.74 (s, 1H), 8.47 (m, 1H), 7.97 (m, 1H), 7.88 (s, 1H), 7.78 (m, 3H), 7.58 (m, 7H), 7.09 (m, 3H), 6.96 (m, 1H), 6.65 (m, 1H), 3.14 (m, 4H), 1.77-0.80 (m, 18H); MS (ES⁺): 609.4 71a —CH═CH₂

67 A-4, I-2, S ¹H NMR (DMSO-d₆): δ 13.80 (br s, 1H), 9.91 (s, 1H), 9.41 (s, 1H), 8.63 (m, 2H), 8.07 (s, 1H), 7.98 (s, 1H), 7.60 (m, 8H), 6.90 (m, 3H), 5.94 (d, J=17.7Hz, 1H), 4.37 (m, 1H), 4.16 (m, 1H), 2.41-1.58 (m, 12H); MS (ES⁺): 537.4 71b —CH═CH₂

67 A-4, I-2, S ¹H NMR (DMSO-d₆): δ 9.76 (s, 1H), 9.41 (s, 1H), 8.95 (s, 1H), 8.53 (m, 1H), 8.07 (s, 1H), 7.65 (m, 8H), 7.08 (m, 2H), 6.85 (dd, J=10.9 and 17.7Hz, 1H), 6.92 (m, 3H), 5.97 (d, J=17.7Hz, 1H), 5.37 (d, J=10.9Hz, 1H), 2.84 (m, 1H), 2.70 (m, 1H), 0.98-0.51 (m, 8H); MS (ES⁺): 509.4 71c —CH═CH₂

67 A-4, I-2, S ¹H NMR (DMSO-d₆): δ 12.51 (br s, 1H), 9.59 (s, 1H), 9.22 (s, 1H), 8.79 (s, 1H), 8.58 (t, J=5.5Hz, 1H), 8.17 (s, 1H), 7.67 (m, 8H), 7.12 (m, 2H), 6.86 (dd, J=10.9 and 17.7Hz, 1H), 5.98 (d, J=17.7Hz, 1H), 5.38 (d, J=I0.9Hz, 1H), 3.27 (m, 4H), 1.20 (t, J=7.2Hz, 1H), 1.09 (t, J=7.2Hz, 1H); MS (ES⁺): 485.3

Cpd. Starting Method No. —R —R′ From Used Analytical Data 68a —CH₃

67 A-4 MS(ES⁺): 599.4 68b —CH₃

67 A-4 MS(ES⁺): 641.4 68c —CH₃

67 A-4 MS(ES⁺): 625.3 68d —CH₃

67 A-4 MS(ES⁺): 583.3 68e —CH₃

67 A-4 MS(ES⁺): 585.3 68f —CH₃

67 A-4 MS(ES⁺): 599.4 68g —CH₃

67 A-4 MS(ES⁺): 625.2 68h —CH₃

67 A-4 MS(ES⁺): 619.2 68i —CH₃

67 A-4 MS(ES⁺): 615.3 68j —CH₃

67 A-4 MS(ES⁺): 597.3 68k —CH₃

67 A-4 MS(ES⁺): 557.3 68l —CH₃

67 A-4 MS(ES⁺): 571.4 68m —CH₃

67 A-4 MS(ES⁺): 639.4 68n —CH₃

67 A-4 Characterized in the next step 68o —CH₃

67 A-4 MS(ES⁺): 613.5 68p —CH₃

67 A-4 MS(ES⁺): 613.5 68q —CH₃

67 A-4 MS(ES⁺): 641.5 68r —CH₃

67 A-4 MS(ES⁺): 714.5 68s —CH₃

67 A-4 MS(ES⁺): 611.4 68t —CH₃

67 A-4 MS(ES⁺): 641.4 68u —CH₃

67 A-4 MS(ES⁺): 583.3 68v —CH₃

67 A-4 MS(ES⁺): 597.4 68w —CH₃

67 A-4 MS(ES⁺): 587.4 68x —CH₃

67 A-4 MS(ES⁺): 613.5 68y —CH₃

67 A-4 MS(ES⁻): 627.3 68z —CH₃

67 A-4 MS(ES⁺): 613.2 68aa —CH₃

67 A-4 MS(ES⁺): 686.2 68ab —CH₃

67 A-4 MS(ES⁺): 617.3 68ac —CH₃

67 A-4 MS(ES⁺): 614.3

-R (Position with Cpd. Respect to Phenyl Starting Method No. Ring) -R′ -R″ X From Used Analytical Data 74 —OCH₃ (3) —CHO —CH₃ CH 73 + 3a D-2 MS (ES⁻): 368.2 75a —OH (3) —CHO —CH₃ CH 74 V-2, W MS (ES⁻): 354.1 75b —OH (3) —CHO —Bn CH 74 V-1, H MS (ES⁻): 430.2 76a —OSO₂CF₃ (3) —CHO —CH₃ CH 75a B-2 MS (ES⁺): 488.1 76b —OSO₂CF₃ (3) —CHO —Bn CH 75b B-2 MS (ES⁻): 562.3 ; MS (ES⁺): 586.3 (M + Na)⁺ 77a —CH═CH₂ (3) —CHO —CH₃ CH 76a D-3 MS (ES⁺): 366.38 77b —OCH₂CO₂C₂H₅ (3) —CHO —Bn CH 75b X Characterized in the next step 77c —OCH₂CONH₂ (3) —CHO —Bn CH 75b X MS (ES⁻): 487.3; MS (ES⁺): 511.35 (M + Na)⁺ 77d

—CHO —Bn CH 76b D-2 Characterized in the next step 77e

—CHO —Bn CH 75b D-8 MS (ES⁺): 530.3 (M + Na)⁺); MS (ES⁻): 506.3 77f

—CHO —Bn CH 75b X MS (ES⁺): 496.3 (M + Na)⁺ 77g

—CHO —Bn CH 75b X MS (ES⁺): 482.4 (M + Na)⁺ 77h

—CHO —Bn CH 75b X MS (ES⁺): 510.4 (M + Na)⁺ 77i

—CHO —Bn CH 75b X ¹HNMR (CDCl₃): δ 9.59 (s, 1H), 8.39(d,J=2 Hz, 1H), 8.03 (m, 2H), 7.84 (d,J=8.9 Hz, 1H), 7.35(d, J=8 Hz, 1H), 1H), 7.28(m, 2H), 7.12(m, 2H), 6.93(dd, J=2.5 and 8.8 Hz, 1H), 6.64(d, J=2.5 Hz, 1H), 6.31 (t, J= 6 and 5 Hz, #1H), 5.06(m, 2H), 4.42(t, J= 4.5 Hz, 2H), 4.13(m, 2H), 3.34(t, J=6.8 Hz, 2H), 2.11(s, 3H), 1.94(m, 1H), 1.01(d, J= 6.8 Hz, 6H) 78a —CH═CH₂ (3) —CO₂H —CH₃ CH 77a E MS (ES⁻): 380.1 78b —OSO₅CF₃ (3) —CO₂H —Bn CH 76b E Characterized in the next step 78c —OCH₂CO₂ C₂H₅(3) —CO₂H —Bn CH 77b E Characterized in the next step 78d —OCH₂CONH₂ (3) —CO₂H —Bn CH 77c E MS (ES⁺): 527.35 (M + Na)⁺ 78e

—CO₂H —Bn CH 77d E MS (ES⁺): 536.4 (M + Na)⁺ 78f

—CO₂H —Bn CH 77e E MS (ES⁻): 522.3 78g —OCH₃ (3) —CO₂H —CH₃ CH 74 E MS (ES⁻): 384.1 78h

—CO₂H —Bn CH 77f E MS (ES⁻): 488.3 78i

—CO₂H —Bn CH 77g E MS (ES⁻): 474.4 78j

—CO₂H —Bn CH 77h E MS (ES⁻): 502.4 78k

—CO₂H —Bn CH 77i E Characterized in the next step 90 —OBn (5) —CHO —CH₃ CH 89 + 3a D-2 ¹HNMR (CDCl₃): δ 10.47(s, 1H), 8.36(d, J=2 Hz, 1H), 7.96(dd, J=2.2 and 7.7 Hz, 1H), 7.68(m, 2H), 7.46(m, 5H), 7.23(d, J=8 Hz, 1H), 7.12(d, J=8.7 Hz, 1H), 6.73 (d, J=7.2 Hz, 1H), 5.23(q, J= 11 and 15 Hz, 2H), 3.67(s, #3H), 3.31(t, J=6.8 Hz, 2H), 1.94(m, 1H), 1.01(d, J=6.8 Hz, 6H), MS (ES+) 468.2 (M + Na)⁺(ES−) 444.2 91 —OBn (5) —CO₂H —CH₃ CH 90 E ¹HNMR (CDCl₃): δ 8.22(s, 1H), 7.83(d, J=7.2 Hz, 1H), 7.34(m, 8H), 7.02(d, J=8.1 Hz, 1H), 6.75(d, J=7.4 Hz, 1H), 5.16(s, 2H), 3.66(s, 3H), 3.21(t, J=6.8 Hz, 2H), 1.85 (m, 1H), 0.94(d, J=6.8 Hz, 6H), MS (ES+) 484.1 (M + Na)⁺ 92 —OBn (5) —CO₂MEM —CH₃ CH 91 F MS (ES⁺): 572.2(M + Na)⁺ 93 —OH (5) —CO₂MEM —CH₃ CH 92 G MS (ES⁺): 482.(M + Na)⁺ 94 —OSO₂CF₃ (5) —CO₂MEM —CH₃ CH 93 B-2 MS (ES⁺): 614.3 (M + Na)⁺ 95a

—CO₂MEM —CH₃ CH 94 D-3 MS (ES⁺) 562.3 (M + Na)⁺ 96a

—CO₂H —CH₃ CH 95a I-1 MS (ES⁺) 452.1 (M + Na)⁺ 101 —OCH₃ (2) —CHO —CH₃ CH 100 + 3a D-2 MS (ES⁺) 370.1 102 —OCH₃ (2) —CO₂H —CH₃ CH 101 E MS (ES⁻) 384.2; MS (ES⁺) 386.2 108 —OBn (2) —CHO —CH₃ CH 107 + 3a D-2 MS (ES⁺): 446.2 109 —OBn (2) —CO₂H —CH₃ CH 108 E MS (ES⁻): 460.1 131 —H —CHO —CH₃ CH 130 + 3a D-2 ¹HNMR (CDCl₃-d₁): δ 9.79(s, 1H), 8.39(d, J=1.88 Hz, 1H), 8.02(t, J=6.0 Hz, 2H), 7.59(m, 2H), 7.38(d, J=7.9 Hz, 1H), 7.22(d, J=8.1 Hz, #1H), 6.30(b, 1H), 3.72(s, 3H), 3.36(t, J=6.6 Hz, 2H), 1.96 (m, 1H), 1.02(d, J=6.8 Hz, 6H), MS (ES⁺): 340.1 132 —H —CO₂H —CH₃ CH 131 E ¹HNMR (DMSO-d₆): δ 12.28 (b, 1H), 8.52(d, J=6.03 Hz, 1H), 8.12(s, 1H), 7.86(d, J= 8.1 Hz, 1H), 7.74(d, J=7.74 Hz, 1H), 7.41(t, J=8.67 Hz, 1 H), 7.31(t, J=7.9 Hz, 1H), 7.12(d, J=8.1 Hz, 1H), 6.97 #(d, J=7.5 Hz, 1H), 3.39(s, 3H), 2.92(t, J=6.0 Hz, 2H), 1.66(m, 1H), 0.78(d, J=7.4 Hz, 6H), MS (ES−): 354.1 193a —H

—CH₃ CH 192a + 6a D-7 MS (ES⁺): 560.5 193b —H

—CH₃ CH 192b + 6a D-7 MS (ES⁺): 574.5) 194a —H

—CH₃ CH 193a S-2 MS (ES⁺): 460.3 194b —H

—CH₃ CH 193b S-2 MS (ES⁺): 474.3 195a —H

—H CH 194a I-2 ¹HNMR (DMSO-d₆): δ 8.79 (bs, 4H), 8.63(t, J=6.5 Hz, 1H), 8.35(s, 1H), 7.85(d, J=6 Hz, 1H), 7.62(d, J=8.2 Hz, 2H), 7.26(m, 5H), 7.06(m, 1H), 5.0(m, 2H), 3.09(t, J= 6.2 Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.6 Hz, 6H); MS (ES−): 444.3 and (ES⁺) 446.3 195b —H

—H CH 194b I-2 ¹HNMR (DMSO-d₆/DCl): δ 8.24(d, J=1.6 Hz, 1H), 7.91 (dd, J=7.7 and 1.6 Hz, 1H), 7.56(d, J=8.7 Hz, 1H), 7.48 (d, J=8.7 Hz, 1H), 7.32(t, J= 8 Hz, 1H), 7.16(m, 3H), 6.91 (t, J=7.5 Hz, 1H), 6.76(d, J= 8.5 Hz, 1H), 6.66(d, J=8.5 #Hz, 1H), 4.99(m, 1H), 2.92 (d, J=6.9 Hz, 2H), 1.68(m, 1H), 1.33(d, J=6 Hz, 1.2 H), 1.27(d, J=6 Hz, 1.8 H), 0.71 (d, J=6.5 Hz, 6H); MS (ES−): 458.2 and (ES⁺) 460.3 200 —H

—CH₃ CH 199 + 6a D-7 MS (ES⁺): 573.5 201 —H

—H CH 200 I-2 ¹HNMR (DMSO-d₆/DCl): δ 8.49(t, J=5.6 Hz, 1H), 8.18 (d, J=6.9 Hz, 1H), 7.84(t, J= 7.8 Hz, 1H), 7.23(m, 4H), 7.01(m, 2H), 6.82(d, J=7 Hz, 1H), 6.22(d, J=8.5 Hz, 1H), 6.15(d, J=8.5 Hz, 1H), 3.95(m, 1H), 2.85(t, J=5.8 #Hz, 1H), 1.62(m, 1H), 1.23 (s, 9H), 1.1(d, J=6.7 Hz, 1.2H), 1.05(d, J=6.7 Hz, 1.8H), 0.67(d, J=6.6 Hz, 6H); MS (ES⁺): 559.4 202 —H

—H CH 201 S MS (ES⁺): 459.3 203 —OBn (4)

—CH₃ CH 45 R MS (ES⁺): 679.4 204 —OBn (4)

—H CH 203 I-2 MS (ES⁻): 663.4 209a —H

—CH₃ CH 132 A-7 MS (ES⁻): 454.3 209b —CH═CH₂ (4)

—CH₃ CH 30f A-7 ¹HNMR (DMSO-d₆): δ 10.72 (s, 1H), 8.65(d, J=6.03 Hz, 1H), 8.24(s, 1H), 8.03(d, J= 8.1 Hz, 1H), 7.75(m, 6H), 7.40(d, J=7.90 Hz, 1H), 7.34 (d, J=8.1 Hz, 1H), 6.88(q, J= 11.2 Hz, 1H), 6.04(d, J= 7.5 Hz, 1H), 5.41(d, J=11.1 #Hz, 1H), 3.55(s, 3H), 3.10(t, J=6.6 Hz, 2H), 1.86(m, 1H), 0.88(d, J=6.6 Hz, 6H); MS (ES⁻): 480.3 209c —CH═CH₂ (4)

—CH₃ N 227 A-7 MS (ES⁻) : 481.4 210b —CH═CH₂ (4)

—CH₃ CH 209b Y ¹HNMR (DMSO-d₆): δ 10.12 (s, 1H), 9.37(b, 1H), 8.48(t, J=6.1 Hz, 1H), 8.05(d, J=1.9 Hz, 1H), 7.85(d, J=7.9 Hz, 1H), 7.56(d, J=7.8 Hz, 1H), 7.49(d, J=7.9 Hz, 1H), 7.36(s, 4H), 7.21(d, J=7.9 Hz, 1H), #1H), 7.10(d, J=2.8 Hz, 1H), 6.69 (m, 1H), 5.84(d, J=15.5 Hz, 1H), 5.60(b, 1H), 5.22(d, J=11.4 Hz, 1H), 3.38(s, 3H), 2.91(t, J=6 Hz, 2H), 1.66(m, 1H), 0.71(d, J=6.8 Hz, 6H); MS (ES+) 515.40 210c —CH═CH₂ (4)

—CH₃ N 209c Y ¹H NMR (DMSO-d₆): δ 10.50 (s, 1H), 9.54(s, 1H), 8.58(t, J=6.4 Hz, 1H), 8.21-7.34(m, 9H), 6.90(dd, J=11.1 and 17.3 Hz, 1H), 6.07(d, J=17.3 Hz, 1H), 5.74(s, 2H), 5.45(d, J=11.1 Hz, 1H), 3.60(s, 3H), #3.16(t, J=6.2 Hz, 2H), 1.88 (m, 1H), 0.88(d, J=6.4 Hz, 6H); MS (ES⁺): 516.40. 211b —CH═CH₂ (4)

—H CH 210b I-2 ¹HNMR (DMSO-d₆): δ 12.62 (bs, 1H), 10.24(s, 1H), 8.48(t, J=5.65 Hz, 1H), 8.15(s, 1H), 7.81(d, J=10.9 Hz, 1H), 7.61 (s, 1H), 7.50(d, J=7.9 Hz, #1H), 7.49(s, 6H), 7.16(d, J=8.1 Hz, 1H),7.08(d, J=8.1 Hz, 1H), 6.72(m, 1H), 5.85(d, J=13.7 Hz, 1H), 5.24(d, J=11.5 Hz, 1H), 2.93(t, J= 6 Hz, 2H), 1.68(m, 1H), 0.72 (d, J=6.8 Hz, 6H); MS (ES+) 501.40, (ES−) 499.2 211c —CH═CH₂ (4)

—H N 210c I-2 ¹H NMR (DMSO-d₆): δ 9.50 (s, 1H), 8.68(m, 1H), 7.93- 7.40(m, 10H), 7.13(m, 2H), 6.86(dd, J=11.1 and 17.3 Hz, 1H), 5.99(d, J=17.3 Hz, 1H), 5.69(s, 1H), 5.38(d, J= 11.1 Hz, 1H), 3.14(t, J=6.2 #Hz, 2H), 1.86(m, 1H), 0.88 (d, J=6.4 Hz, 6H); MS (ES⁺): 500.36. 212 —CH═CH₂ (4)

—CH₃ CH 187a AE-5 ¹H NMR (DMSO): δ 8.70(t, J= 5.6 Hz, 1H), 8.36(d, J=1.7 Hz, 1H), 8.07(dd, J=8.1, 1.9 Hz, 1H), 7.42(m, 4H), 7.09(d, J=5.5 Hz, 1H), 7.04(d, J= 7.7 Hz, 1H), 6.74(dd, J= 17.5, 10.9 Hz, 1H), 6.49(d, J= #8.8 Hz, 2H), 5.79(d, J= 17.7 Hz, 1H), 5.27(d, J=10.9 Hz, 1H), 4.0(t, J=6.0 Hz, 2H), 3.62(s, 3H), 3.11(t, J= 6.2, 2H), 1.86(m, 1H), 0.90 (d, J=6.6 Hz, 6H) 212a —CH═CH₂ (4)

—CH₃ N 247 AE-5 MS (ES⁺) 469.3 212b —CH═CH₂ (4)

—CH₃ CH 187a AE-5 characterized in the next step 213 —CH═CH₂ (4)

—CH₃ CH 212 Y ¹H NMR (DMSO): δ 9.23(s, 1H), 8.71(t, J=6.2 Hz, 1H), 8.36(d, J=1.9 Hz, 1H), 8.09 (dd, J=7.9, 1.7 Hz, 1H), 7.49 (d, J=7.9 Hz, 2H), 7.40(d, J= 8.3 Hz, 1H), 7.32(d, J=8.8 Hz, 2H), 7.04(d, J=7.9 Hz, 1H), 6.73(dd, J=17.7, 11.1 Hz, #1H), 6.40(d, J=8.5 Hz, 2H), 6.33(t, J=7.0 Hz, 1H), 5.78 (d, J=17.7 Hz, 1H), 5.58(b, 1H), 5.26(d, J=11.1 Hz, 1H), 3.96(m, 2H), 3.64(s, 3H), 3.11(t, J=6.4 Hz, 2H), 1.86 (m, 1H), 0.90(d, J=6.8 Hz, 6H); MS (ES⁺): 501.3 213a —CH═CH₂ (4)

—CH₃ N 212a Y ¹H NMR (DMSO-d₆): δ 8.98 (s, 1H), 8.46(t, J=6.4 Hz, 1H), 7.96(d, J=8.0 Hz, 1H), 7.87(d, J=8.0 Hz, 1H), 7.31 (s, 1H), 7.21(d, J=8.1 Hz, 2H), 7.09(d, J=8.5 Hz, 1H), 6.88(d, J=7.9 Hz, 1H), 6.51 (dd, J=11.1 and 17.3 Hz, 1H), #6.15(m, 3H), 5.58(d, J=17.3 Hz, 1H), 5.30(s, 1H), 5.06(d, J=11.1 Hz, 1H), 3.77(m, 2H), 3.42(s, 3H), 2.93(t, J= 7.0 Hz, 2H), 1.67(m, 1H), 0.66(d, J=6.4 Hz, 6H); MS (ES⁺): 502.35. 213b —CH═CH₂ (4)

—CH₃ CH 212b Y ¹HNMR (DMSO-d₆): δ 9.4(bs, 1H), 8.70(k, J=5.5 Hz, 1H), 8.35(d, J=1.7 Hz, 1H), 8.17 (d, J=2.5 Hz, 1H), 8.47(dd, J= 8.1, 2 Hz, 1H), 7.58(dd, J= 8.8, 2.5 Hz, 1H), 7.47(m, 1H, 2H), 7.38(d, J=7.2 Hz, 1H), #7.07(t, J=5 Hz, 1H), 7.03(d, J=7.7 Hz, 1H), 6.73(dd, J= 11.17 Hz, 1H), 6.41(d, J=8.8 Hz, 1H), 5.80(d, J=17 Hz, 1H), 5.78(bs, 2H), 5.21(d, J= 11 Hz, 1H), 4.16(d, J=5.3 Hz), 3.62(s, 3H), 3.15(t, J= 6.78 Hz, 2H), 1.87(m, 1H), 0.91(d, J=6.7 Hz, 6H); MS (ES⁺) 502.46. 214 —CH═CH₂ (4)

—H CH 213 I-2 ¹H NMR (DMSO): δ 8.76(t, J= 5.8 Hz, 1H), 8.37(s, 1H), 8.04(d, J=8.7 Hz, 1H), 7.39 (m, 5H), 7.06(d, J=8.3 Hz, 1H), 6.72(dd, J=17.9, 11.3 Hz, 1H), 6.43(d, J=8.5 Hz, 3H), 5.76(d, J=17.9 Hz, 1H), 5.24 #(d, J=11.1 Hz, 1H), 3.98(m, 2H), 3.11(t, J=6.6 Hz, 2H), 1.86(h, J=6.8 Hz, 1H), 0.90 (d, J=6.8, 6H); MS (ES⁺): 487.2 214a —CH═CH₂ (4)

—H N 213a I-2 ¹H NMR (DMSO-d₆): δ 9.33 (s, 1H), 8.98(t, J=6.4 Hz, 1H), 8.16(d,J=8.0 Hz, 1H), 8.00(d, J=8.0 Hz, 1H), 7.51 (s, 1H), 7.41(d, J=8.1 Hz, 1H), 7.31(d, J=8.5 Hz, 2H), 7.11(d, J=7.9 Hz, 1H) 6.75 #(dd, J=11.1 and 17.3 Hz, 1H), 6.46(m, 3H), 5.80(d J=17.3 Hz, 1H), 5.72(s, 2H) 5.27(d, J=11.1 Hz, 1H), 3.97(s, 2H), 2.93(t, J=7.0 Hz, 2H), 1.90 (m, 1H), 0.90(d, J=6.4 Hz, 6H); MS (ES⁺): 488.36. 214b —CH═CH₂ (4)

H CH 213b I-2 ¹HNMR (DMSO-d₆): δ 8.69(t, J=6 Hz, 1H), 8.35(1, 1H), 8.63(s, 1H), 8.03(d, J=8 Hz, 1H), 7.60(d, J =9 Hz, 1H), 7.47(s, 1H), 7.41(m, 3H), 7.06(d, J=7.7 Hz, 1H), 6.75 (dd, J=10.5, 17.5 H, 1H), 6.47(d, J=7 Hz, 1H), 5.80(d, #J=17 Hz, 1H), 5.27(d, J= 10.5 Hz, 1H), 4.21(m, 2H), 3.10(t, J=6.7 Hz, 2H), 2.07 (s, 3H), 1.87(m, 1H), 0.90(d, J=6.5 Hz, 6 H); MS (ES⁺) 488.39. 238 —CH═CH₂ (4)

—H CH 237 + 187a AE-2 ¹HNMR (DMSO-d₆): δ 8.68- 8.60(m, 1H), 8.50(d, J=2.4 Hz, 1H), 7.90-7.80(m, 1H), 7.76-7.70(m, 1H), 7.56-7.50 (m, 1H), 7.48-7.42(d, J=7.7 Hz, 1H), 7.30-7.22(d, J=7.9 Hz, 1H), 7.10-7.02(d, J=7.7 Hz, 1H), 6.90-6.75(dd, J=17, #11 Hz, 1H), 6.5 (bs, 1H), 5.92-5.80(d, J=17 Hz, 1H), 5.40-5.30(d, 11 Hz, 1H), 4.50- 4.20(m, 2H), 3.20-3.10(t, J= 6.6 Hz, 2H), 2.10-1.88(m, 1H), 1.2-0.94(d, J=6.6 Hz, 6H); MS (ES⁺) 471.3 256 —H

—CH₃ CH 255 + 6a D-6 MS (ES⁺): 573.3 257 —H

—H CH 256 I-2, S MS (ES⁺): 459.1

Cpd. Starting Method No. —R —R′ From Used Analytical Data 79a —CH═CH₂ (3) —CH₃ 78a J MS(ES⁺): 499.2 79b —OSO₂CF₃ (3) —CH₂C₆H₅ 78b J Characterized in the next step 79c —OCH₂CO₂C₂H₅ (3) —CH₂C₆H₅ 78c J Characterized in the next step 79d —OCH₂CONH₂ (3) —CH₂C₆H₅ 78d J MS(ES⁺): 622.4; (ES⁻)620.4 79e

—CH₂C₆H₅ 78e J Characterized in the next step 79f

—CH₂C₆H₅ 78f J Characterized in the next step 79g —OCH₃ (3) —CH₃ 78g J ¹HNMR(DMSO-d₆): δ10.6(bs, 1H), 9.29-9.32(bs, 1H), 9.06(bs, 1H), 8.82-8.75(t, J=5.84Hz, 1H), 8.32(d, J= 1.88Hz, 1H), 8.13(d, J=1.7Hz, 1H), 7.83(s, 4H), 7.78(d, J=8.67Hz, 1H), 7.50(d, J=7.9Hz, 1H), 7.20-7.15(dd, J= 8.67, 2.3Hz, 1H), 6.92(d, J=2.4Hz, 1H), 3.94(s, 3H), 3.64(s, 3H), 3.21-3.14(t, J=6Hz, 2H), 2.0-1.86(m, 1H), 1.0-0.94(d, J=6.5Hz, 6H); MS(ES⁺)503.3 79h

—Bn 78h J MS(ES⁺): 607.3 79i

—Bn 78i J MS(ES⁺): 593.4 79j

—Bn 78j J MS(ES⁺): 621.4 79k —O—CH₂—CH₂—OAc (3) —Bn 78k J MS(ES⁺): 651.4 80a —CH═CH₂ (3) —H 79a I-2 ¹HNMR(DMSO-d₆): δ9.1(s, 2H), 8.87(s, 2H), 8.53(t, J= 6Hz, 1H), 8.02(s, 1H), 7.64(m, 7H), 7.1(s, 1H), 6.98(d, 7.4Hz, 1H), 6.80(dd, J=11Hz, J=17.6Hz, 1H), 5.90(d, J= 17.6Hz, 1H), 5.35(d, J=12Hz, 1H), 3.03(t, 6Hz, 2H), 1.83(m, 1H), 0.86(d, J=6.7Hz, 6H); MS(ES⁺)485.2 80b —OH (3) —H 79b I-2 ¹HNMR(DMSO-d₆): δ10.37(s, 1H), 9.20(m, 3H), 8.72(t, J=6Hz, 1H), 8.2(s, 1H), 8.85(m, 6H), 7.65(d, J=8Hz, 1 H), 7.12(d, 8Hz, 1H), 7.02(dd, J=2.5Hz, J=8Hz, 1H), 6.60(d, J=2.5Hz, 1H), 3.25(t, J=6.5Hz, 2H), 2.0(m, 1 H), 1.07(d, J=6.8Hz, 6H); MS(ES⁺)475.2 80c —OCH₂CO₂H (3) —H 79c I-2 ¹HNMR(DMSO-d₆): δ12.7(2H, bs, 1H), 9.01, 8.87(2bs, 4 H), 8.36(m, 1H), 7.83(s, 1H), 7.44(m, 6H), 6.75(m, 2H), 6.31(d, J=2.2Hz, 1H), 4.42(s, 2H), 2.84(m, 2H), 1.63(m, 1H), 0.67(d, J=6.5Hz, 6H); MS(ES+): 533.4 ¹HNMR(DMSO-d₆): δ9.13(bs, 5H), 8.59(t, J═6.28Hz, 80d —OCH₂CONH₂ (3) —H 79d G ¹H NMR(DMSO-d₆): δ9.13(bs, 5H), 8.59(t, J=6.28Hz, 1H), 8.14(d, J=1.7Hz, 1H), 7.63(m, 9H), 7.42(s, 1H), 7.09 (d, J=7.5Hz, 1H), 7.03(dd, J=2.5, 12.7Hz, 1H), 6.70(d, J= 2.5Hz, 1H), 4.48(s, 2H), 3.05(t, J=6.6Hz, 2H), 1.83(m, 1H), 0.87(d, J=6.8Hz, 6H); MS(ES+): 532.4 80e

—H 79e I-2 ¹HNMR(DMSO-d₆): δ12.6(1H, bs, COOH), 8.98, 8.67(2 bs, 4H), 8.46(m, 1H), 8.08(m, 1H), 7.76(m, 1H), 7.53(m, 6 H), 7.39(m, 2H), 7.06(m, 1H), 7.04(m, 1H), 2.89(m, 2H), 1.66(m, 1H), 0.69(d, J=6.5Hz, 6H); MS(ES+): 541.4 80f

—H 79f I-2 ¹HNMR(DMSO-d₆): δ9.14(d, J=10Hz, 4H), 8.60(t, J=6 Hz, 1H), 8.22(bs, 1H), 7.87-7.62(m, 7H), 7.47(t, J=8Hz, 2H), 7.26(t, 7Hz, 1H), 7.22(m, 4H), 6.70(bs, 1H), 3.09(t, J=6Hz, 2H), 1.83(m, 1H), 0.91(d, J=6.8Hz, 6H); MS (ES⁺)551.4 80g —OCH₃ (3) —H 79g I-2 ¹HNMR(DMSO-d₆): δ9.13(bs, 2H), 8.78(bs, 2H), 8.65(t, J= 6Hz, 1H), 8.25(bs, 1H), 7.78(m, 1H), 7.76(m, 5H), 7.25(s, 1H), 7.17(m, 1H), 6.73(bs, 1H), 3.83(s, 3H), 3.10 (t, J=6Hz, 2H), 1.80(m, 1H), 0.88(d, J=6.8Hz, 6H); MS(ES⁺)489.3 80h

—H 79h I-2 MS(ES⁺): 517.7 80i

—H 79i I-2 MS(ES⁺): 503.4; MS(ES⁻): 501.4 80j

—H 79j I-2 MS(ES⁺): 531.4; MS(ES⁻): 529.4 80k —O—CH₂—CH₂—OH (3) —H 79k I-2 ¹HNMR(DMSO-d₆): δ13.52(bs, 1H), 9.16(bs, 2H), 9.03 (bs, 2H), 8.50(t, J=6Hz, 1H), 7.96(d, J=1.7Hz, 1H), 7.56(m, 6H), 7.00(dd, J=2.5 and 8.5Hz, 1H), 6.90(d, J= 8Hz, 1H), 6.48(d, J=2.5Hz, 1H), 4.91(t, J=5.5Hz, 1H), 4.00(t, J=4.5Hz, 2H), 3.69(q, J=5.5 and 10Hz, 2H), 3.05(t, J=6.8Hz, 2H), 1.80(m, 1H), 0.84(d, J=6.8Hz, 6 H); MS(ES⁺): 519.3, (ES−)517.3 86a —CH(OH)CH₂OH (3) —H 82 S, I-2 ¹HNMR(DMSO-d₆): δ9.15(bs, 3H), 8.65(t, J=6Hz, 1H), 8.12(s, 2H), 7.82-7.56(m, 7H), 7.55-6.96(m, 4H), 5.5(bs, 1H), 4.90(bs, 1H), 4.65(bs, 1H), 3.10(t, J=6Hz, 2H), 1.90(m, 1H), 0.92(d, J=6.8Hz, 6H); MS(ES⁺)519.3 86b —CH₂OH (3) —H 84 S, I-2 ¹HNMR(DMSO-d₆): δ8.82(bs, 2H), 8.68(bs, 2H), 8.40(t, J=6Hz, 1H), 7.88(bs, 1H), 7.53(m, 5H), 7.45(d, 8Hz, 1 H), 7.25(d, J=8Hz, 1H), 6.81(m, 2H), 5.22(d, J=5.5Hz, 1H), 4.41(d, J=5.5Hz, 2H), 2.88(t, J=6Hz, 2H), 1.65(m, 1H), 0.71(d, J=6.8Hz, 6H); MS(ES⁺)489.2 86c —CO₂H (3) —H 85 S, I-2 ¹HNMR(DMSO-d₆-D₂O): δ13.7(bs, 1H), 8.32(t, J=6Hz, 1H), 7.63-7.17(m, 7H), 6.72(d, 7.0Hz, 1H), 2.81(t, J=6 Hz, 2H), 1.53(m, 1H), 0.64(d, J=6.8Hz, 6H); MS(ES⁺) 503.2 97a

—CH₃ 96a J MS(ES⁺): 569.2 97b —OBn (5) —CH₃ 91 J ¹HNMR(DMSO-d₆): δ10.62(s, 1H), 9.15(bs, 2H), 8.82 (bs, 2H), 8.67(t, J=6Hz, 1H), 8.25(d, J=2Hz, 1H), 7.99 (dd, J=8.1 and 2Hz, 1H), 7.69(q, 8.8 and 16.2Hz, 4H), 7.44(m, 3H), 7.28(m, 3H), 6.89(d, J=7.7Hz, 1H), 5.5(s, 2H), 3.6(s, 3H), 3.08(t, J=5.8 and 6.8Hz, 2H), 1.83(m, 1 H), 0.87(d, J=6.8Hz, 6H); MS(ES−)577.2, (ES+)579.3 98a

—H 97a I-2 ¹HNMR(DMSO-d₆): δ13.45(bs, 1H), 9.06(s, 2H), 8.99(s, 2H), 8.51(t, J=6 and 5Hz, 1H), 7.99(s, 1H), 7.62(m, 5 H), 7.47(s, 1H), 7.36(m, 2H), 6.99(m, 4H), 4.26(s, 2H), 3.02(t, J=6.8Hz, 2H), 1.80(m, 1H), 0.86(d, J=6.8Hz, 6 H); MS(ES−)553.2, (ES+)555.2 98b —OBn (5) —H 97b I-2 ¹HNMR(DMSO-d₆): δ13.52(bs, 1H), 9.09(bs, 2H), 9.04 (bs, 2H), 8.48(t, J=6Hz, 1H), 7.94(s, 1H), 7.61(m, 4H), 7.49(s, 1H), 7.46(s, 1H), 7.34(m, 5H), 7.15(d, J=8.2Hz, 1H), 7.00(d, J=8.2, 1H), 6.02(d, J=7.4Hz, 1H), 5.21(s, 2H), 3.01(t, J=6.8Hz, 2H), 1.80(m, 1H), 0.85(d, J=6.8 Hz, 6H); MS(ES−)563.2, (ES+)565.2 98c —OH (5) —H 98b G ¹HNMR(DMSO-d₆): δ9.85(s, 1H), 9.07(s, 2H), 8.98(s, 2 H), 8.50(t, J=6 and 5Hz, 1H), 7.99(d, J=1.7Hz, 1H), 7.63(m, 5H), 7.20(t, J=8Hz, 2H), 6.90(d, J=7.9Hz, 1 H), 6.49(d, J=7.2Hz, 1H), 3.21(t, J=6.8Hz, 2H), 1.80 (m, 1H), 0.85(d, J=6.8Hz, 6H); MS(ES+)475.2; (ES−) 473.2 103 —OCH₃ (2) —CH₃ 102 J MS(ES+)503.1 104 —OCH₃ (2) —H 103 I-2 ¹HNMR(DMSO-d₆): δ9.08(bs, 2H), 8.80(bs, 2H), 8.52(t, J=6Hz, 1H), 8.02(s, 1H), 7.64(m, 5H), 7.16(m, 2H), 7.03(m, 2H), 3.84(s, 3H), 3.03(t, J=6.8Hz, 2H), 1.81(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES−)487.3, (ES+)489.3 110 —OBn (2) —CH₃ 109 J MS(ES⁺): 579.3 111 —OH (2) —CH₃ 110 G MS(ES⁺): 489.3 126

—CH₃ 118b J Characterized in the next step 127

—H 126 I-2 ¹HNMR(DMSO-d6): δ9.06-9.09(m, 3H), 8.56-8.50(m, 1H), 8.05(s, 1H), 7.71-7.58(m, 6H), 7.55-7.28(m, 6H), 7.10- 7.01(m, 1H), 6.63(s, 1H), 5.19(s, 2H), 4.05-3.97(m, 2H), 3.05-3.01(m, 2H), 1.86-1.77(m, 1H), 1.29(t, J=6.7Hz, 3H), 0.87(d, J=6.8Hz, 6H) 129

—H 128 I-2, S ¹HNMR(DMSO-d₆): 13.64(br s, 1H), 8.99(br s, 2H), 8.49 (t, J=5.1Hz, 1H), 7.99(s, 1H), 7.73-7.56(m, 5H), 7.32- 6.83(m, 5H), 6.50(s, 1H), 5.17(d, J=4.3Hz, 1H), 5.01 (m, 1H), 3.75(s, 3H), 3.03(t, J═6.0Hz, 1H), 1.81(m, 1 H), 1.32(d, J=6.2Hz, 3H), 0.86(d, J=6.6Hz, 6H); MS (ES⁺): 533.4(100% M⁺¹)

Cpd. —R (With Respect to Starting Method No. Phenyl Ring) From Used Analytical Data 81 —CH═CH₂ (3) 79a R MS (ES⁻): 597.2 82 —CH(OH)CH₂OH (3) 81 L MS (ES⁻¹): 631.3 83 —CH═O (3) 82 M MS (ES⁺): 601.3 84 —CH₂OH (3) 83 K MS (ES⁻¹): 601.4 85 —CO₂H (3) 83 E MS (ES⁻¹): 615.3 128 

124a R MS (ES⁺): 629.4

Cpd. Starting Method No. —R —R1 —R2 —R3 —R4 From Used Analytical Data  88 —Br —H —H —H —OBn 87 X ¹H NMR (CDCl₃): δ 10.48(s, 1H), 7.42- 7.25(m, 7H), 7.00(dd, J=2 and 7.4 Hz, 1H), 5.19(s, 2H); IR (KBr) 1701, 1585, 1452, 1262, 1009 cm⁻¹; MS (ES+) 313.0, 315.0(M + Na)⁺  89 —B(OH)₂ —H —H —H —OBn 88 T, U-1 ¹H NMR (CDCl₃): δ 10.61(s, 1H), 7.65 (d, J=7.2Hz, 1H), 7.60(t, J=7.9 and 7.2Hz, 1H), 7.41(m, 5H), 7.19(d, J= 7.9Hz, 1H), 6.81(bs, 2H), 5.20(s, 2H) 100 —B(OH)₂ —OCH₃ —H —H —H 99 T, U-3 ¹H NMR (DMSO-d₆): δ 10.2(s, 1H), 8.34(s, 2H), 7.92(d, J=9.4Hz, 1H), 7.13(m, 2H), 3.92(s, 3H); MS (ES⁻) 179.0 107 —B(OH)₂ —OBn —H —H —H 106  T, U-1 ¹H NMR (DMSO-d6): δ 10.1(s, 1H), 7.3-7.6(m, 8H), 5.3(m, 2H) 114a —Br —H —OCH₃ —OH —H 113  Z MS (ES⁻): 229.0 and 231.0 114b —Br —H —OC₂H₅ —OH —H 113  Z-1 MS (ES⁻): 242.9 and 244.9 114c —Br —H —OCH(CH₃)₂ —OH —H 113  Z-1 MS (ES⁻): 257.0 and 259.0 115a —Br —H —OCH₃ —OBn —H 114a X MS (ES⁺): 321.0 and 323.0 115b —Br —H —OC₂H₅ —OBn —H 114b X MS (ES⁺): 335.0 and 337.0 115c —Br —H —OCH(CH₃)₂ —OBn —H 114c X MS (ES⁺): 349.0 and 351.0 115d —Br —H

—OBn —H 115a X, V-4, AH Characterized in the next step 116a —B(OH)₂ —H —OCH₃ —OBn —H 115a T, U-1 Characterized in the next step 116b —B(OH)₂ —H —OC₂H₅ —OBn —H 115b T, U-1 Characterized in the next step 116c —B(OH)₂ —H —OCH(CH₃)₂ —OBn —H 115c T, U-1 Characterized in the next step

Cpd. Starting Method No. From Used Analytical Data 112 111 I-2 ¹H NMR (DMSO-d₆): δ 11.28(s, 1H), 9.31(s, 2H), 9.0(s, 2H), 8.88(d, J=11.30Hz, 1H), 8.82(d, J=1.88Hz, 1H), 8.25(d, J=1.88Hz, 1H), 8.18(d, J=1.88Hz, 1H), 8.04(d, J=8.47Hz, 1H), 7.92(m, J=24.48Hz, 2H), 7.75(m, J=15.82, 1H), 7.75(m, J=8.28Hz, 1H), 7.55(m, J=8.66Hz, 1H), 3.10(m, J=12.6Hz, 1H), 2.5(m, J=3.5Hz, 1H), 1.8(m, J=19.9Hz, 2H), 0.88(m, J=6.6Hz, 6H).

Cpd. Starting Method No. —R —R′ —R″ —R′′′ From Used Analytical Data 117a —CH₃ —OBn —CHO

3a + 116a D-2 MS (ES⁻): 474.2 117b —C₂H₅ —OBn —CHO

3a + 116b D-2 MS (ES⁻): 488.2 117c —CH(CH₃)₂ —OBn —CHO

3a + 116c D-2 MS (ES⁻): 502.3 117d —CH₃ —OBn —CHO

3b + 116a D-2 ¹H NMR (CDCl₃): δ 9.56(s, 1 H), 8.34(d, J=1.7Hz, 1H), 8.5 (s, 1H), 8.01(dd, J=7.9 and 1.9 Hz, 1H), 7.40(m, 7H), 6.9(s, 1 H), 5.24(m, 2H), 4.2(m, 1H), 3.80(s, 3H), 3.52(s, 3H), 1.02 (d, J=7Hz, 6H); MS (ES+): 484.3(M + Na)⁺ 117e —CH₃ —OBn —CHO

3c + 116a D-2 ¹H NMR (DMSO-d₆): δ 8.43(d, J= 1.65Hz, 1H), 8.31(d, J=8.66 Hz, 1), 8.12(dd, J=1.69Hz, 1H), 7.98(s, 1H), 7.41(d, J=8 and 10Hz, 1H), 7.19(d, J=8.1 Hz, 1H), 5.20(dd, J=6.2Hz, 1H), 3.98(dd, J=7.75Hz, 3H), 3.94(s, 3H), 3.42(m, 3H), 3.32 (m, 3H), 3.19(s, 3H), # 2.5(m, 3H), 2.0(s, 4H), 1.5(m, 2H), 1.28(m, 3H), 0.88(d, J=6.59 Hz, 3H); MS (ES+): 664.3 117f —CH₃ —OBn —CHO

3d + 116a D-2 ¹H NMR (CDCl₃): δ 9.50(s, 1 H), 8.40(d, J=2.1Hz, 1H), 8.04 (dd, J=8.1, 2.1Hz, 1H), 7.57(s, 1H), 7.48(m, 5H), 7.38(m, 5 H), 6.67(s, 1H), 6.50(broad, 1 H), 5.27(d, J=11.9Hz, 1H), 5.22(dd, J=11.7, 1H), 4.63(m, 3H) 4.17(m, 4H), 3.92 (s, 3H), 3.66(s, 3H); # MS (ES⁻): 488.3 117g —CH₃ —OBn —CHO

3f + 116a D-2 ¹H NMR (CDCl₃): δ 9.50(s, 1 H), 8.40(d, J=2.1Hz, 1H), 8.04(dd, J=8.1, 2.1Hz, 1H), 7.57(s, 1H), 7.48(m, 2H), 7.38 (m, 3H), 6.67(s, 1H), 6.50 (broad, 1H), 5.27(d, J=11.9 Hz, 1H), 5.22(dd, J=11.7, 2 H), 4.17(m, 2H), 3.92(s, 3H), 3.66(s, 3H); MS (ES⁻): 500 117h —CH₃ —OBn —CHO

3e + 116a D-2 ¹H NMR (CDCl₃): δ 9.56(s, 1 H), 8.34(d, J=1.7Hz, 1H), 8.01(dd, J=7.9, 1.9Hz, 1H), 7.57(s, 1H), 7.50(dd, J=7.2, 1.5, 2H), 7.40(m, 4H), 6.67(s, 1H), 6.21(broad, 1H), 5.24(d, J= 2.8Hz, 2H), 3.92(s, 3H), 3.65 (s, 3H), 3.52(m, 2H), 1.65(m, 2 H), 1.46(m, 2H), 0.99(t, # J=7.3 Hz, 3H). 117i —CH₃ —OBn —CHO

3g + 116a D-2 ¹H NMR (CDCl₃): δ 9.57(s, 1 H), 8.37(d, J=1.9Hz, 1H), 8.03(dd, J=7.9, 1.9Hz, 1H), 7.58(s, 1H), 7.50(d, J=7.2Hz, 2H), 7.38(m, 3H), 6.68(s, 1H), 6.33(broad, 1H), 5.26(d, J= 11.5Hz, 1H), 5.21(d, J=11.9 Hz, 1H), 3.92(s, 3H), 3.65(s, 3 H), 3.37(dd, J=7.2, # 5.3Hz, 2 H), 1.09(m, 1H), 0.60(m, 2H), 0.32(m, 2H); MS (ES⁺): 474.2 117j —CH₃ —OBn —CHO

3h + 116a D-2 ¹H NMR (CDCl₃): δ 9.55(s, 1 H), 8.32(d, J=1.9Hz, 1H), 8.00(dd, J=1.9 and 7.9Hz, 1 H), 7.59-7.30(m, 7H), 6.67(s, 1 H), 5.23(m, 2H), 4.45(q, J=7.0 Hz, 1H), 3.91(s, 3H), 3.64(s, 3 H), 2.21-1.46(m, 8H); MS (ES⁺): 510.3(M + Na)⁺ 117k —CH₃ —OBn —CHO

3i + 116a D-2 ¹H NMR (CDCl₃): δ 9.56(s, 1 H), 8.35(d, J=1.9Hz, 1H), 8.02(dd, J=1.9 and 7.9Hz, 1 H), 7.58-7.33(m, 7H), 6.68(s, 1 H), 5.24(m, 2H), 3.92(s, 3H), 3.65(s, 3H), 3.56(m, 2H), 1.30 (t, J=7.2Hz, 3H); MS (ES⁺): 470.3(M + Na)⁺ 117l —CH₃ —OBn —CHO

3j + 116a D-2 ¹H NMR (CDCl₃): δ 9.56(s, 1 H), 8.35(d, J=1.9Hz, 1H), 8.02(dd, J=1.9 and 7.9Hz, 1 H), 7.58-7.33(m, 7H), 6.68(s, 1 H), 5.24(m, 2H), 3.92(s, 3H), 3.65(s, 3H), 3.40(m, 2H), 1.80- 0.94(m, 9H); MS (ES⁺): 512.2 (M + Na)⁺ 117m

—OBn —CHO

6a + 115d D-6 ¹H NMR (DMSO-d₆): δ 9.73(s, 1 H), 8.86(t, J=5.7Hz, 1H), 8.52 (d, J=1.5Hz, 1H), 8.22(dd, J= 8 and 2Hz, 1H), 7.79(s, 1H), 7.60(d, J=8Hz, 1H), 7.5(m, 5 H), 7.22(s, 1H), 5.35(q, J=11 and 17Hz, 1H), 3.70(s, 3H), 3.23(t, J=6.5Hz, 2H), 1.98(m, 1H), 1.3(s, 9H), 1.01(d, # J=6.8 Hz, 6H); MS (ES⁺): 546.4 118a —CH₃ —OBn —CO₂H

117a E MS (ES⁻): 490.2 118b —C₂H₅ —OBn —CO₂H

117b E MS (ES⁻): 504.2 118c —CH(CH₃)₂ —OBn —CO₂H

117c E MS (ES⁻): 518.2 118d —CH₃ —OBn —CO₂H

117d E Characterized in the next step 118e —CH₃ —OBn —CO₂H

117e E MS (ES⁺): 534.3 118f —CH₃ —OBn —CO₂H

117f E MS (ES⁺): 506.3 118g —CH₃ —OBn —CO₂H

117g E Characterized in the next step 118h —CH₃ —OBn —CO₂H

117h E MS (ES⁻¹): 490.2 118i —CH₃ —OBn —CO₂H

117i E MS (ES⁻¹): 488.3 118j —CH₃ —OBn —CO₂H

117j E ¹H NMR (DMSO-d₆): δ 12.19 (br s, 1H), 8.50(d, J=7.4Hz, 1 H), 8.31(d, J=1.9Hz, 1H), 8.02(dd, J=1.7 and 7.9Hz, 1 H), 7.58-7.29(m, 7H), 6.71(s, 1 H), 5.17(s, 2H), 4.27(q, J=6.4 Hz, 1H), 3.80(s, 3H), 3.57(s, 3 H), 1.97-1.51(m, 8H) 118k —CH₃ —OBn —CO₂H

117k E MS (ES⁻): 462.3 118l —CH₃ —OBn —CO₂H

117l E ¹H NMR (CDCl₃): δ 8.30(d, J= 1.9Hz, 1H), 7.95(dd, J=1.7 and 7.9Hz, 1H), 7.66(s, 1H), 7.52-7.27(m, 6H), 6.62(s, 1H), 6.49(m, 1H), 5.21(s, 2H), 3.88 (s, 3H), 3.61(s, 3H), 3.38(m, 2 H), 1.79-0.94(m, 9H); MS (ES⁻): 504.4 118m

—OBn —CO₂H

117m E Characterized in the next step 119a —CH₃ —OBn —CO₂MEM

118a F MS (ES⁻): 578.3 119b —C₂H₅ —OBn —CO₂MEM

118b F MS (ES⁻): 592.3 119c —CH(CH₃)₂ —OBn —CO₂MEM

118c F MS (ES⁻): 606.3 119d —CH₃ —OBn —CO₂MEM

118d F MS (ES⁻): 564.2 119e —CH₃ —OBn —CO₂MEM

118e F MS (ES⁻): 620.1 119f —CH₃ —OBn —CO₂MEM

118f F MS (ES⁻): 592.3 119g —CH₃ —OBn —CO₂MEM

118g F Characterized in the next step 119h —CH₃ —OBn —CO₂MEM

118h F ¹H NMR (CDCl₃): δ 8.32(d, J= 1.9Hz, 1H), 7.96(dd, J=7.9, 1.9Hz, 1H), 7.68(s, 1H), 7.50 (m, 2H), 7.35(m, 4H), 6.62(s, 1 H), 6.33(t, J=5.4Hz, 1H), 5.24 (m, 4H), 3.88(s, 3H), 3.63(s, 3 H), 3.46(m, 6H), 3.34(s, 3H), 1.63(m, 2H), 1.44(m, 2H), 0.98 (t, J=7.3Hz, 3H) 119i —CH₃ —OBn —CO₂MEM

118i F ¹H NMR (CDCl₃): δ 8.34(d, J= 1.9Hz, 1H), 8.00(dd, J=7.9, 2.1Hz, 1H), 7.68(s, 1H), 7.50 (m, 2H), 7.36(m, 4H), 6.63(s, 1 H), 6.42(broad, 1H), 5.24(m, 4 H), 3.89(s, 3H), 3.64(s, 3H), 3.45(s, 3H), 3.35(m, 5H), 1.07 (m, 1H), 0.58(m, 2H), 0.30(m, 2H) 119j —CH₃ —OBn —CO₂MEM

118j F ¹H NMR (DMSO-d₆): δ 8.55(d, J=7.4Hz, 1H), 8.39(d, J=1.9 Hz, 1H), 8.10(dd, J=1.7 and 7.9Hz, 1H), 7.63-7.35(m, 7H), 6.81(s, 1H), 5.25-5.12(m, 4H), 4.31(q, J=6.4Hz, 1H), 3.86(s, 3H), 3.62(s, 3H), 3.3(s, 3H), 3.23(s, 3H) 1.99-1.53(m, 8H); MS (ES⁺): 614.3(M + Na)⁺ 119k —CH₃ —OBn —CO₂MEM

118k F ¹H NMR (DMSO-d₆): δ 8.70(t, J=5.5Hz, 1H), 8.35(d, J=1.9 Hz, 1H), 8.05(dd, J=1.7 and 7.9Hz, 1H), 7.59-7.30(m, 7H), 6.77(s, 1H), 5.21-5.08(m, 4H), 3.82(s, 3H), 3.58(s, 3H), 3.40- 3.29(m, 6H), 3.18(s, 3H), 1.14 (t, J=7.2Hz, 3H); MS (ES⁺): 574.3(M + Na)⁺ 119l —CH₃ —OBn —CO₂MEM

118l F ¹H NMR (DMSO-d₆): δ 8.68(t, J=5.8Hz, 1H), 8.35(d, J=1.9 Hz, 1H), 8.05(dd, J=1.7 and 7.9Hz, 1H), 7.63-7.33(m, 7H), 6.77(s, 1H), 5.22-5.08(m, 4H), 3.82(s, 3H), 3.58(s, 3H), 3.39- 3.22(m, 6H), 3.18(s, 3H), 1.56 (qui, J=7.0Hz, 2H), 1.27(m, 1 H), 0.94-0.75(m, # 6H); MS (ES⁺): 616.3(M + Na)⁺ 119m

—OBn —CO₂MEM

118m F ¹H NMR (DMSO-d₆): δ 8.72(t, J= 5.6Hz, 1H), 8.38(d, J=1.8 Hz, 1H), 8.70(dd, J=1.8 and 8.1Hz, 1H), 7.71(s, 1H), 7.40 (m, 6H), 7.02(s, 1H), 5.20(m, 4 H), 3.59(s, 3H), 3.37(m, 2H), 3.31(m, 2H), 3.17(s, 3H), 3.12 (t, J=6.5Hz, 2H), 1.87(m, 1 H), 1.21(s, 9H), 0.91(d, # J=6.8 Hz, 6H); MS (ES+): 650.4 and 672.3(M + Na)⁺ 120a —CH₃ —OH —CO₂MEM

119a G MS (ES⁻): 488.1 120b —C₂H₅ —OH —CO₂MEM

119b G MS (ES⁻): 502.2 120c —CH(CH₃)₂ —OH —CO₂MEM

119c G MS (ES⁻): 516.3 120d —CH₃ —OH —CO₂MEM

119d G MS (ES⁻): 474.3 120e —CH₃ —OH —CO₂MEM

119e G MS (ES⁻): 530.4 120f —CH₃ —OH —CO₂MEM

119f G MS (ES⁻): 502.3 120g —CH₃ —OH —CO₂MEM

119g G Characterized in the next step 120h —CH₃ —OH —CO₂MEM

119h G Characterized in the next step 120i —CH₃ —OH —CO₂MEM

119i G MS (ES⁻): 486.3 120j —CH₃ —OH —CO₂MEM

119j G MS (ES⁺): 524.3(M + Na)⁺ 120k —CH₃ —OH —CO₂MEM

119k G MS (ES⁺): 484.2(M + Na)⁺ 120l —CH₃ —OH —CO₂MEM

119l G MS (ES⁻): 502.3 120m

—OH —CO₂MEM

119m G ¹H NMR (DMSO-d₆): δ 10.83(bs, 1H), 8.77(t, J=5.6Hz, 1H), 8.42(d, J=1.8Hz, 1H), 8.12 (dd, J=1.8 and 8.1Hz, 1H), 7.68(s, 1H), 7.41(d, J=8.1Hz, 1H), 6.73(s, 1H), 5.21(q, J= 21 and 6Hz, 2H), 3.65(s, 3H), 3.48(m, 2H), 3.37(m, 2H), 3.24 (s, 3H), 3.18(t, J=6.5Hz, # 2H), 1.94(m, 1H), 1.39(s, 9H), 0.97 (d, J=6.8Hz, 6H); MS (ES+): 560.5 and 582.4(M + Na)⁺, (ES⁻) 558.4 121a —CH₃ —OSO₂CF₃ —CO₂MEM

120a B-2 MS (ES⁺): 644.1(M + Na)⁺ 121b —C₂H₅ —OSO₂CF₃ —CO₂MEM

120b B-2 MS (ES⁺): 658.2(M + Na)⁺ 121c —CH(CH₃)₂ —OSO₂CF₃ —CO₂MEM

120c B-2 MS (ES⁺): 672.2(M + Na)⁺ 121d —CH₃ —OSO₂CF₃ —CO₂MEM

120d B-2 ¹H NMR (DMSO-d₆): δ 8.43(d, J= 1.9Hz, 1H), 8.31(s, 1H), 8.12 (d, J=1.69Hz, 1H), 7.98(s, 1 H), 7.41(d, J=8.1Hz, 1H), 7.19 (s, 1H), 5.20(m, 2H), 3.98(m, 1 H), 3.94(s, 3H), 3.42(s, 3H), 3.19(s, 3H), 2.50(m, 2H), 1.08 (d, J=6.59, 6H); MS (ES+) 608.3 121e —CH₃ —OSO₂CF₃ —CO₂MEM

120e B-2 ¹H NMR (DMSO-d₆): δ 8.49(s, 1 H), 8.34(d, J=1.8Hz, 1H), 8.2 (d, J=1.8Hz, 1H), 7.97(s, 1H), 7.4(d, J=7.8Hz, 1H), 7.2(s, 1 H), 5.2(q, J=6 and 10Hz, 2H), 4.0(m, 3H), 3.6(s, 3H), 3.4(m, 4H), 3.2(s, 3H), 1.5(m, 4H), 1.3(m, 4H), 0.85(m, 6H); MS (ES+): 664.3 121f —CH₃ —OSO₂CF₃ —CO₂MEM

120f B-2 ¹H NMR (DMSO-d₆): δ 8.83(d, J= 5.46, 1H), 8.55(d, J=1.88Hz, 1H), 8.23(dd, J=1.88Hz, 1H), 8.19(s, 1H), 7.73(d, J=7.93 Hz, 1H), 7.29(s, 1H), 5.29(dd, J=6.217Hz, 2H), 4.06(s, 3H), 3.71(s, 2H), 3.54(m, 5H), 2.62 (t, J=3.57Hz, 3H), 1.66(t, J= 6.59Hz, 2H), 1.42(m, # 6H), 0.99(t, J=6.79Hz, 3H); MS (ES+) 636.6 121g —CH₃ —OSO₂CF₃ —CO₂MEM

120g B-2 ¹H NMR (CDCl₃): δ 8.43(d, J= 1.9Hz, 1H), 8.03(dd, J=7.9 Hz, 2.1Hz, 1H), 8.00(s, 1H), 7.35(d, J=7.9Hz, 1H), 6.79 (m, 2H), 5.29(d, J=6.2Hz, 1 H), 5.26(d, J=6.2Hz, 1H), 4.16(m, 2H), 3.94(s, 3H), 3.67 (s, 3H), 3.48(m, 4H), 3.36(s, 3 H); MS (ES⁻): 646.3 121h —CH₃ —OSO₂CF₃ —CO₂MEM

120h B-2 ¹H NMR (CDCl₃): δ 8.41(s, 1 H), 7.96(d, J=8.3Hz, 2H), 7.8 (m, 1H), 6.80(s, 1H), 6.34(m, 1H), 5.32(m, 2H), 3.90(s, 3 H), 3.66(s, 3H), 3.55(m, 6H), 3.4(s, 3H), 1.7(m, 2H), 1.45 (m, 2H), 0.98(t, J=7.3Hz, 3 H); MS (ES⁻): 620 121i —CH₃ —OSO₂CF₃ —CO₂MEM

120i B-2 ¹H NMR (CDCl₃): δ 8.41(d, J= 2.1Hz, 1H), 8.03(dd, J=7.9, 1.9Hz, 1H), 8.00(s, 1H), 7.32 (d, J=7.9Hz, 1H), 6.43(t, J= 4.9Hz, 1H), 5.30(q, J=6.0Hz, 2H), 3.94(s, 3H), 3.67(s, 3H), 3.55(m, 2H), 3.48(m, 2H), 3.35 (m, 5H), 1.09(m, 1H), 0.59(m, 2H), 0.31(m, 2H); # MS (ES⁻): 618.4 121j —CH₃ —OSO₂CF₃ —CO₂MEM

120j B-2 ¹H NMR (CDCl₃): δ 8.35(d, J= 1.9Hz, 1H), 8.00(m, 2H), 7.31 (d, J=7.9Hz, 1H), 6.77(s, 1H), 6.27(m, 1H), 5.28(m, 2H), 4.44 (q, J=7.0Hz, 1H), 3.94(s, 3H), 3.66(s, 3H), 3.57-3.45(m, 4H), 3.35(s, 3H), 2.19-1.45(m, 8H); MS (ES⁺): 656.3(M + Na)⁺ 121k —CH₃ —OSO₂CF₃ —CO₂MEM

120k B-2 ¹H NMR (CDCl₃): δ 8.38(s, 1 H), 8.00(m, 2H), 7.31(d, J=7.9 Hz, 1H), 6.78(s, 1H), 6.37(m, 1 H), 5.27(m, 2H), 3.94(s, 3H), 3.66(s, 3H), 3.59-3.43(m, 6H), 3.35(s, 3H), 1.28(t, J=7.2Hz, 3H); MS (ES⁺): 616.3(M + Na)⁺ 121l —CH₃ —OSO₂CF₃ —CO₂MEM

120l B-2 ¹H NMR (CDCl₃): δ 8.38(s, 1 H), 8.00(m, 2H), 7.31(d, J=7.9 Hz, 1H), 6.78(s, 1H), 6.37(m, 1 H), 5.27(m, 2H), 3.94(s, 3H), 3.66(s, 3H), 3.57-3.25(m, 9H), 1.78-0.92(m, 9H); MS (ES⁺): 658.4(M + Na)⁺ 121m

—OSO₂CF₃ —CO₂MEM

121m B-2 ¹H NMR (DMSO-d₆): δ 8.75(t, J= 5.6Hz, 1H), 8.45(d, J=1.8 Hz, 1H), 8.11(dd, J=1.8 and 8.1Hz, 1H), 8.04(s, 1H), 7.57 (s, 1H), 7.42(d, J=8.1Hz, 1H), 5.23(q, J=21 and 6Hz, 2H), 3.60(s, 3H), 3.41(m, 2H), 3.32 (m, 2H), 3.17(s, 3H), 3.13(t, J= 6.5Hz, 2H), 1.87(m, # 1H), 1.37(s, 9H), 0.91(d, J=6.8Hz, 6H); MS (ES−): 690.4 122a —CH₃ —CH═CH₂ —CO₂MEM

121a D-3 Characterized in the next step 122b —C₂H₅ —CH═CH₂ —CO₂MEM

121b D-3 MS (ES⁺): 536.3(M + Na)⁺ 122c —CH(CH₃)₂ —CH═CH₂ —CO₂MEM

121c D-3 MS (ES⁺): 550.3(M + Na)⁺ 122d —CH₃ —CH═CH₂ —CO₂MEM

121d D-3 MS (ES⁺): 486.2 122e —CH₃ —CH═CH₂ —CO₂MEM

121e D-3 MS (ES⁺): 564.5(M + Na)⁺ 122f —CH₃ —CH═CH₂ —CO₂MEM

121f D-3 MS (ES⁺): 514.4(M + Na)⁺ 122g —CH₃ —CH═CH₂ —CO₂MEM

121g D-3 Characterized in the next step 122h —CH₃ —CH═CH₂ —CO₂MEM

121h D-3 Characterized in the next step 122i —CH₃ —CH═CH₂ —CO₂MEM

121i D-3 Characterized in the next step 122j —CH₃ —CH═CH₂ —CO₂MEM

121j D-3 MS (ES⁻): 422.3[(M − MEM)−1] 122k —CH₃ —CH═CH₂ —CO₂MEM

121K D-3 MS (ES⁺): 494.2(M + Na)⁺ 122l —CH₃ —CH═CH₂ —CO₂MEM

121l D-3 MS (ES⁺): 536.42(M + Na)⁺ 122m

—CH═CH₂ —CO₂MEM

121m D-3 ¹H NMR (DMSO-d₆): δ 8.73(t, J= 5.6Hz, 1H), 8.43(d, J=1.8 Hz, 1H), 8.11(dd, J=1.8 and 8.1Hz, 1H), 7.61(s, 1H), 7.57 (s, 1H), 7.42(d, J=8.1Hz, 1H), 6.72(dd, J=11 and 17.5Hz, 1 H), 6.03(d, J=17.5Hz, 1H), 5.52(d, J=11Hz, 1H), 5.19(q, J=18 and 6Hz, 2H), # 3.60(s, 3 H), 3.41(m, 2H), 3.32(m, 2H), 3.18(s, 3H), 3.13(t, J=6.5Hz, 2H), 1.89(m, 1H), 1.38(s, 9H), 0.91(d, J=6.8Hz, 6H); MS (ES−): 480.4[(M − MEM)−1] 123a —CH₃ —CH═CH₂ CO₂H

122a I-1 MS (ES⁻): 410.2 123b —C₂H₅ —CH═CH₂ CO₂H

122b I-1 MS (ES⁻): 424.2 123c —CH(CH₃)₂ —CH═CH₂ CO₂H

122c I-1 MS (ES⁻): 438.2 123d —CH₃ —CH═CH₂ CO₂H

122d I-1 MS (ES⁻): 396.2 123e —CH₃ —CH═CH₂ CO₂H

122e I-1 MS (ES⁺): 454.3 123f —CH₃ —CH═CH₂ CO₂H

122f I-1 MS (ES⁺): 426.3 123g —CH₃ —CH═CH₂ CO₂H

122g I-1 ¹H NMR (DMSO): δ 12.37(s, 1 H), 9.35(t, J=6.0Hz, 1H), 8.42 (d, J=1.7Hz, 1H), 8.10(dd, J= 8.1Hz, 1.9Hz, 1H), 8.06(s, 1 H), 7.40(d, J=7.9Hz, 1H), 6.98(dd, J=17.9, 11.5Hz, 1H), 6.77(s, 1H), 5.89(dd, J=17.7, 1.3Hz, 1H), 5.37(dd, J=11.1, 1.3Hz, 1H), 4.14(m, 2H), # 3.84 (s, 3H), 3.61(s, 3H); MS (ES⁻): 436.3 123h —CH₃ —CH═CH₂ CO₂H

122h I-1 ¹H NMR (DMSO): δ 8.66(t, J= 5.5Hz, 1H), 8.35(d, J=1.7Hz, 1H), 8.05(s, 1H), 8.03(dd, J= 8.1, 1.9Hz, 1H), 7.34(d, J=7.9 Hz, 1H), 6.98(dd, J=17.9, 11.3 Hz, 1H), 6.75(s, 1H), 5.88(dd, J=17.7, 1.3, 1H), 5.36(dd, J= 11.3, 1.3Hz, 1H), 3.84(s, 3H), 3.60(s, 3H), 3.30(q, # J=5.6Hz, 2H), 1.52(m, 2H), 1.33(m, 2 H), 0.96(t, J=7.3Hz, 3H); MS (ES⁻): 410.4 123i —CH₃ —CH═CH₂ CO₂H

122i I-1 ¹H NMR (DMSO): δ 12.34(s, 1 H), 8.80(t, J=6.1Hz, 1H), 8.37 (d, J=1.9Hz, 1H), 8.06(dd, J= 9.8, 7.9Hz, 1H), 8.05(s, 1H), 7.36(d, J=7.9Hz, 1H), 6.98 (dd, J=17.9, 11.3Hz, 1H), 6.76 (s, 1H), 5.89(dd, J=17.9, 1.5 Hz, 1H), 5.36(dd, J=10.9, 1.5 Hz, 1H), 3.84(s, 3H), # 3.60(s, 3 H), 3.18(t, 6.2, 2H), 1.06(m, 1 H), 0.45(m, 2H), 0.25(m, 2H); MS (ES⁻): 408.4 123j —CH₃ —CH═CH₂ CO₂H

122j I-1 ¹H NMR (DMSO-d₆): δ 12.31 (br s, 1H), 8.52(d, J=7.3Hz, 1 H), 8.34(d, J=1.7Hz, 1H), 8.05(m, 2H), 7.34(d, J=7.9 Hz, 1H), 6.97(dd, J=11.5 and 17.9Hz, 1H), 6.74(s, 1H), 5.89 (d, J=17.9Hz, 1H), 5.37(d, J= 11.5Hz, 1H), 4.27(q, J=7.3 Hz, 1H), 3.84(s, 3H), # 3.60(s, 3 H), 1.98-1.50(m, 8H); MS (ES⁻): 422.3 123k —CH₃ —CH═CH₂ CO₂H

122k I-1 ¹H NMR (DMSO-d₆): δ 12.27 (br s, 1H), 8.58(m, 1H), 8.23(s, 1H), 7.92(m, 2H), 7.47(m, 1 H), 7.22(m, 1H), 6.84(m, 1H), 6.63(s, 1H), 5.76(d, J=17.9 Hz, 1H), 5.24(d, J=11.5Hz, 1 H), 3.71(s, 3H), 3.47(s, 3H), 1.02(m, 3H); MS (ES⁻): 382.2 123l —CH₃ —CH═CH₂ CO₂H

122l I-1 ¹H NMR (DMSO-d₆): δ 12.30 (br s, 1H), 8.52(d, J=6.0Hz, 1 H), 8.33(d, J=1.7Hz, 1H), 8.02(m, 2H), 7.31(d, J=7.9 Hz, 1H), 6.95(dd, J=11.5 and 17.9Hz, 1H), 6.73(s, 1H), 5.86 (d, J=17.9Hz, 1H), 5.33(d, J= 11.5Hz, 1H), 3.81(s, 3H), 3.57 (s, 3H), 3.14(m, 2H), # 1.65(m, 1 H), 1.39(m, 1H), 1.11(m, 1H), 0.87(m, 6H) 123m

—CH═CH₂ —CO₂H

122m I-1 ¹H NMR (DMSO-d₆): δ 12.81(bs, 1H), 8.72(t, J=5.6Hz, 1H), 8.38(d, J=1.8Hz, 1H), 8.08 (dd, J=1.8 and 8.1Hz, 1H), 7.61(s, 1H), 7.57(s, 1H), 7.39 (d, J=8Hz, 1H), 6.72(dd, J= 11 and 17.5Hz, 1H), 5.99(d, J= 17.5Hz, 1H), 5.49(d, J=11Hz, 1H), 3.57(s, 3H), 3.13(t, # J= 6.5Hz, 2H), 1.87(m, 1H), 1.37 (s, 9H), 0.91(d, J=6.8Hz, 6H); MS (ES−): 480.3

Cpd. Starting Method No. —R —R′ R″ From Used Analytical Data 124a —CH₃ —CH₃

123a J MS (ES⁺): 529.3 124b —C₂H₅ —CH₃

123b J MS (ES⁺): 543.3 124c —CH(CH₃)₂ —CH₃

123c J MS (ES⁺): 557.3 124d —CH₃ —CH₃

123d J Characterized in the next step 124e —CH₃ —CH₃

123e J MS (ES⁺): 571.6 124f —CH₃ —CH₃

123f J MS (ES⁺): 543.6 124g —CH₃ —CH₃

123g J ¹H NMR (DMSO): δ 10.62(s, 1H), 9.35(t, J=6.6 Hz, 1H), 9.20(s, 2H), 8.90(s, 2H), 8.30(d, J= 1.9Hz, 1H), 8.11(dd, J=8.1, 1.9Hz, 1H), 7.86 (s, 1H), 7.76(s, 4H), 7.50(d, J=8.1Hz, 1H), 7.04(dd, J=17.9, 11.5Hz, 1H), 6.94(s, 1H), 6.01(dd, J=17.7, 1.3, 1H), 5.42(dd, J=11.3, 1.3 Hz, 1H), 4.11(m, 2H), 3.89(s, 3H), 3.57(s, 3H) 124h —CH₃ —CH₃

123h J ¹H NMR (DMSO): δ 9.03(broad, 3H), 8.49 (broad, 1H), 8.04(s, 1H), 7.65(m, 6H), 6.99(m, 2H), 6.61(s, 1H), 5.90(d, J=17.5Hz, 1H), 5.35 (d, J=11.5Hz, 1H), 3.78(s, 3H), 3.20(m, 2H), 1.46(m, 2H), 1.28(m, 2H), 0.87(t, J=7.3Hz, 3H) 124i —CH₃ —CH₃

123i J MS (ES⁺): 527.4 124j —CH₃ —CH₃

123j J MS (ES⁺): 541.4 124k —CH₃ —CH₃

123K J MS (ES⁺): 501.3 124l —CH₃ —CH₃

123l J MS (ES⁺): 543.3 124m

—CH₃

123m J ¹H NMR (DMSO-d₆): δ 10.67(s, 1H), 9.19(bs, 2 H), 8.88(bs, 2H), 8.71(t, J=5.6Hz, 1H), 8.25 (d, J=1.8Hz, 1H), 8.07(dd, J=1.8 and 8.1Hz, 1 H), 7.73(m, 4H), 7.65(s, 1H), 7.50(d, J=8Hz, 1H), 7.45(s, 1H), 6.73(dd, J=11 and 17.5Hz, 1 H), 6.03(d, J=17.5Hz, 1H), 5.49(d, J=11Hz, 1 H), 3.56(s, 3H), 3.09(t, J=6.5Hz, 2H), # 1.85(m, 1H), 1.37(s, 9H), 0.89(d, J=6.8Hz, 6H); MS (ES−): 597.3 and (ES⁺) 599.5 125a —CH₃ —H

124a I-2 ¹H NMR (DMSO): δ 13.40(bs, 1H), 9.26 and 9.03 (2s, 4H), 8.53-8.49(t, J=6Hz, 1H), 8.02(d, J=1.28Hz, 1H), 7.71-7.53(m, 6H), 7.0-6.9(m, 2H), 6.5(s, 1H), 5.89(d, J=17.6Hz, 1H), 5.33(d, J=12.4Hz, 1H), 3.77(s, 3H), 3.04-2.99(m, 2H), 1.85-1.75(m, 1H), 0.86-0.84(d, J=76.8Hz, 6H); MS (ES⁺): 515.3 125b —C₂H₅ —H

124b I-2 ¹H NMR (DMSO): δ 9.17 and 8.92(s, 3H), 8.67- 8.63(m, 1H), 8.28(s, 1H), 7.95-7.93(m, 1H), 7.83 (s, 1H), 7.73(s, 5H), 7.29(d, J=8.1Hz, 1H), 7.02 (dd, J=17.7Hz, 11.3Hz, 1H), 6.82(s, 1H), 6.00(d, 17.7Hz, 1H), 5.38(d, 11.3Hz, 1H), 4.14-4.06(m, 2H), 3.11-3.04(q, J=6.8Hz, 2H),1.89-1.80(m, 1H), 1.35(t, J=6.8Hz, 3H), # 0.88(d, J=6.8Hz, 6H); MS (ES⁺): 529.2 125c —CH(CH₃)₂ —H

124c I-2 ¹H NMR (DMSO): δ 13.74(s, 1H), 8.99(s, 3H), 8.59-8.41(m, 1H), 7.95(s, 1H), 7.69(s, 1H), 7.65- 7.53(m, 6H), 7.06-6.91(m, 2H), 6.53(s, 1H), 5.89 (d, J=17.7Hz, 1H), 5.32(d, J=11.5Hz, 1H), 4.62- 4.54(m, 1H), 3.03-2.99(m, 2H), 1.87-1.71(m, 1H), 1.25(d, J=6.1Hz, 6H), 0.85(d, J=6.8Hz, 6H); MS (ES⁻): 541.2 125d —CH₃ —H

124d I-2 ¹H NMR (DMSO-d₆): δ 8.9(d, J=33.74, 4H), 8.08(d, J=7.91, 1H), 7.81(s, 1H), 7.51(s, 1H), 7.41(s, 4H), 6.78(s, 1H), 6.3(s, 2H), 5.70(d, J= 7.78Hz, 1H), 5.15(d, J=11.8Hz, 2H), 3.82(m, J=20.34Hz, 2H), 3.56(bs, 3H) 0.92(d, 6H); MS (ES+) 501.3 125e —CH₃ —H

124e I-2 ¹H NMR (DMSO-d₆): δ 9.05(s, 2H), 8.85(s, 2H), 7.96(d, J=9.04Hz, 1H), 7.88(s, 1H), 6.86(m, J= 17.8Hz, 3H), 7.62(m, 1H), 7.24(d, J=7.8Hz, 1H), 6.95(d, J=7.8Hz, 1H), 7.45(m, J=28.63 Hz, 5H), 7.55(s, 1H), 5.75(d, J=17.5Hz, 1H); 5.61(d, J=11.11, 1H) 3.61(s, 3H) 1.30(bs, 3H) 1.05(s, 4H) 0.66(m, 6H); MS (ES+) # 555.3(100% M⁺¹) 125f —CH₃ —H

124f I-2 ¹H NMR (DMSO-d₆): δ 12.7(bs, 1H), 9.01(bs, 2H), 8.87(bs, 2H), 8.36(t, J=6Hz, 1H), 7.83(s, 1H), 7.44(m, 6H), 6.75(m, 2H), 6.31(d, J=2.2 Hz, 1H), 5.7(d, J=17Hz, 1H), 5.1(d, J=11Hz, 1H), 3.5(s, 3H), 2.84(m, 2H), 1.3(m, 2H), 1.1(m, 4H), 0.7(m, 3H); MS (ES+): 529.4 125g —CH₃ —H

124g I-2 ¹H NMR (DMSO): δ 9.22(broad, 1H), 9.09(s, 2 H), 8.9(s, 2H), 8.18(s, 1H), 7.80(m, 2H), 7.66 (m, 4H), 7.16(s, 1H), 7.00(dd, J=17.7, 11.1Hz, 1H), 6.70(s, 1H), 5.94(d, J=17.7Hz, 1H), 5.37 (d, J=10.9Hz, 1H), 4.07(m, 2H), 3.81(s, 3H); MS (ES⁻) 539.3 125h —CH₃ —H

124h I-2 ¹H NMR (DMSO): δ 9.03(bs, 4H), 8.49(bs, 1 H), 8.04(s, 1H), 7.65(m, 6H), 6.99(m, 2H), 6.61(s, 1H), 5.90(d, J=17.5Hz, 1H), 5.35(d, J= 11.5Hz, 1H), 3.78(s, 3H), 3.20(m, 2H), 1.46 (m, 2H), 1.28(m, 2H), 0.87(t, J=7.3Hz, 3H); MS (ES⁺) 515.4 125i —CH₃ —H

124i I-2 ¹H NMR (DMSO): δ 8.86(s, 2H), 8.78(s, 2H), 8.44(broad, 1H), 7.89(s, 1H), 7.53(m, 2H), 7.43(m, 4H), 6.86(s, 1H), 6.78(dd, J=17.5, 11.3Hz, 1H), 6.44(s, 1H), 5.71(d, J=17.5Hz, 1 H), 5.14(d, J=11.1Hz, 1H), 3.59(s, 3H), 2.89 (m, 2H), 0.79(m, 1H), 0.20(m, 2H), 0.01(m, 2 H); MS (ES⁻) 513.4 125j —CH₃ —H

124j I-2 ¹H NMR (DMSO): δ 13.14(br s, 1H), 8.84(m, 3 H), 8.12(d, J=7.3Hz, 1H), 7.79(s, 1H), 7.40 (m, 8H), 6.74(m, 2H), 6.33(s, 1H), 5.66(d, J= 19.2Hz, 1H), 5.10(d, J=11.7Hz, 1H), 3.94(m, 1H), 3.54(s, 3H), 1.66-0.93(m, 8H); MS (ES⁺) 527.4 125k —CH₃ —H

124k I-2 ¹H NMR (DMSO): δ 9.25(m, 4H), 8.73(t, J= 5.7Hz, 1H), 8.28(s, 1H), 7.86(m, 7H), 6.84(s, 1H), 6.10(d, J=17.7Hz, 1H), 5.55(d, J=11.3 Hz, 1H), 3.99(s, 3H), 3.43(qui, J=6.2Hz, 2H), 1.28(t, J=7.2Hz, 3H); MS (ES⁺): 487.2 125l —CH₃ —H

124l I-2 ¹H NMR (DMSO): δ 8.91(m, 4H), 8.38(t, J=5.5Hz, 1H), 7.96(s, 1H), 7.53(m, 5H), 6.86(m, 2H), 6.52 (s, 1H), 5.77(d, J=17.7Hz, 1H), 5.21(d, J=11.5 Hz, 1H), 3.65(s, 3H), 2.94(m, 1H), 1.57-0.56(m, 11 H); MS (ES⁺): 529.3 125m —H —H

124m I-2 ¹H NMR (DMSO-d₆): δ 10.07(bs, 1H), 9.05(bs, 2 H), 8.98(bs, 2H), 8.49(t, J=5.6Hz, 1H), 7.96(s, 1H), 7.62(m, 5H), 7.06(s, 1H), 7.03(s, 1H), 6.94(dd, J=11 and 18Hz, 1H), 5.78(d, J=18 Hz, 1H), 5.26(d, J=11Hz, 1H), 3.02(t, J=5.7 Hz, 2H), 1.81(m, 1H), 0.85(d, J=6.8Hz, 6H); MS (ES−): 499.2 and (ES⁺) 501.3

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 133a

—H —CH₃ 132 A-5 MS(ES⁺): 506.4 133b

—H —CH₃ 132 J MS(ES⁺): 499.3 133c

—H —CH₃ 132 A-5 Characterized in the next step 133d

—H —CH₃ 132 A-5 Characterized in the next step 133e

—H —CH₃ 132 A-5 Characterized in the next step 133f

—H —CH₃ 132 A-5 Characterized in the next step 133g

—H —CH₃ 132 A-5 Characterized in the next step 133h

—H —CH₃ 132 A-5 Characterized in the next step 133i

—H —CH₃ 132 A-5 Characterized in the next step 133j

—H —CH₃ 132 A-5 Characterized in the next step 133k

—H —CH₃ 132 J MS(ES⁺): 502.3 133l

—H —CH₃ 132 J MS(ES⁺): 470.2 133m

—H —CH₃ 132 J MS(ES⁺): 437.3 133n

—H —CH₃ 132 J MS(ES⁺): 518.2 133o

—H —CH₃ 132 J MS(ES⁺): 501.3 133p

—H —CH₃ 132 J MS(ES⁺): 469.1 133q

—H —CH₃ 132 J MS(ES⁺): 469.1; MS(ES⁺): 471.2 133r

—H —CH₃ 132 A-5 Characterized in the next step 133s

—H —CH₃ 132 A-5 MS(ES⁺): 483.2(M+Na) 133u

—H —CH₃ 132 A-5 MS(ES⁺): 432.2 133v

—H —CH₃ 132 A-5 MS(ES⁺): 432.2 133w

—H —CH₃ 132 A-5 MS(ES⁺): 447.2 133x

—H —CH₃ 132 A-5 Characterized in the next step 133y

—H —CH₃ 132 A-5 MS(ES⁺): 446.3 133z

—H —CH₃ 132 A-5 MS(ES⁺): 446.2 133aa

—H —CH₃ 132 A-4 MS(ES⁺): 475.3 133ab

—H —CH₃ 132 J MS(ES⁺): 499.3(M+Na) 133ac

—H —CH₃ 132 A-4 MS(ES⁻): 483.2; MS(ES⁺): 485.2 133ad

—H —CH₃ 132 A-4 MS(ES⁺): 497.2; MS(ES⁻): 495.2 133ae

—H —CH₃ 132 A-4 MS(ES⁻): 483.2; MS(ES⁺): 485.2 133af

—H —CH₃ 132 J MS(ES⁺): 511.3(M+Na)⁺; MS(ES⁻): 487.3 133ag

—H —CH₃ 132 J MS(ES⁻): 451.3 133ai

—H —CH₃ 132 J MS(ES⁻): 584.4 134a

—H —H 133a I-2 ¹HNMR(DMSO-d₆): δ13.13(bs, 1H), 8.76(t, J= 6 and 5Hz, 1H), 8.32(m, 2H), 8.02(dd, J= 1.9 and 8.1Hz, 1H), 7.42(m, 4H), 7.25(m, 1 H), 3.62-3.19(m, 12H), 3.11(t, J=6.8 Hz, 2H), 1.87(m, 1H), 1.76(m, 2H), 0.90(d, J=6.8Hz, 6H); MS(ES−)490.3; (ES+)492.3 134b

—H —H 133b I-2 ¹HNMR(DMSO-d₆): δ13.82(bs, 1H), 10.57 (bs, 2H), 8.50(t, J=6 and 5Hz, 1H), 7.99(d, J= 1.5Hz, 1H), 7.83(s, 1H), 7.8(s, 1H), 7.59 (m, 4H), 7.46(m, 2H), 7.03(m, 1H), 6.92(d, J= 7.9Hz, 1H), 3.89(s, 4H), 3.02(t, J=6.8Hz, 2H), 1.81(m, 1H), 0.8(d, J=6.8Hz, 6H); MS (ES⁻): 483.3; MS(ES⁺): 485.4 134c

—H —H 133c I-2 ¹HNMR(DMSO-d₆): δ8.71(t, J=5.5Hz, 1H), 8.40(t, J=5.3Hz, 1H), 8.30(s, 1H), 8.00(d, J= 7.8Hz, 1H), 7.63(d, J=4.3Hz, 2H), 7.40(d, J=7.4Hz, 4H), 7.27(d, J=8.1Hz, 1H), 7.18(s, 1 H), 6.91(d, J=7.1Hz, 1H), 4.42(b, 2H), 3.13(t, J=6.5Hz, 2H), 1.93(m, 1H), 0.91(d, J=6.8 Hz, 6H); MS(ES−)497.3 134d

—H —H 133d I-2 ¹HNMR(DMSO-d₆): δ10.45(s, 1H), 8.63(s, 1 H), 8.27(s, 1H), 7.93(d, J=8.1Hz, 1H), 7.67(t, J=6.8Hz, 2H), 7.55(m, 2H), 7.27(m 3H), 7.12 (m, 2H), 3.06(t, J=6Hz, 2H), 1.82(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES−)483.3 134e

—H —H 133e I-2 ¹HNMR(DMSO-d₆): δ12.92(bs, 1H), 8.71(t, J=5.8Hz, 1H), 8.49(t, J=6.2Hz, 1H), 8.32(s, 1 H), 8.01(d, J=7.8Hz, 1H), 7.52(m, 5H), 7.27 (d, J=7.9Hz, 1H), 7.18(m, 1H), 7.08(d J=8.2 Hz, 2H), 4.32(d, J=4.2Hz, 2H), 3.12(t, J=6.5 Hz, 2H), 1.88(m, 1H), 0.91(d, J=6.8Hz, 6 H); MS(ES−)498.2 134f

—H —H 133f I-2 ¹HNMR(DMSO-d₆): δ8.66(t, J=5.7Hz, 1H), 8.27(s, 1H), 7.92(d, J=8.1Hz, 1H), 7.45(m, 7 H), 7.18(m, 3H), 4.32(d, J=5.9Hz, 2H), 3.12 (t, J=6Hz, 2H), 1.89(m, 1H), 0.91(d, J=6.8 Hz, 6H); MS(ES−)497.2 134g

—H —H 133g I-2 ¹HNMR(DMSO-d₆): δ13.1(s, 1H), 9.58(s, 1 H), 8.65(s, 1H), 8.29(s, 1H), 7.98(d, J=5.9Hz, 1H), 7.75(d, J=5.2Hz, 2H), 7.30(d, J=8Hz, 2 H), 7.12(d, J=12.0Hz, 1H), 7.12(m, 4H), 3.06 (t, J=6Hz, 2H), 1.85(m, 1H), 0.86(d, J=6.8 Hz, 6H); MS(ES−)483.2 134h

—H —H 133h I-2 ¹HNMR(DMSO-d₆): δ10.31(s, 1H), 8.65(t, J=6.2Hz, 1H), 8.31(s, 1H), 7.98(d, J=7.9Hz, 1H), 7.66(m, 1H), 7.53(m, 3H), 7.27(m, 4H), 6.85(m, 1H), 3.09(t, J=6.5Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.8Hz, 6H); MS(ES−) 433.1(M⁻¹) 134i

—H —H 133i I-2 ¹HNMR(DMSO-d₆): δ8.71(t, J=5.7Hz, 1H), 8.31(s, 1H), 8.01(d, J=7.9Hz, 1H), 7.46(m, 2 H), 7.39(m, 2H), 7.24(s, 1H), 3.38(b, 8H), 3.11(t, J=6.5Hz, 2H), 1.86(m, 1H), 0.91(d, J= 6.8Hz, 6H); MS(ES−)409.3 134j

—H —H 133j I-2 ¹HNMR(DMSO-d₆): δ9.61(s, 1H), 8.67(t, J=5.5Hz, 1H), 8.32(s, 1H), 7.98(d, J=7.9Hz, 1H), 7.71(m, 2H), 7.54(m, 2H), 7.29(d, J=7.9 Hz, 1H), 7.04(m, 4H), 3.10(t, J=6.5Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.8Hz, 6H); MS(ES− )433.3 134k

—H —H 133k I-2 ¹HNMR(DMSO-d₆): δ8.59(t, J=6 and 5Hz, 1 H), 8.3(d, J=5Hz, 2H), 8.18(s, 1H), 7.86(d, J= 8Hz, 1H), 7.36(m, 5H), 6.6(t, J=4.7Hz, 1 H), 4.0(m, 1H), 3.75(m, 2H), 3.37(m, 5H), 3.07(t, J=6.8Hz, 2H), 1.81(m, 1H), 0.85(d, J= 6.8Hz, 6H) 134l

—H —H 133l I-2 ¹HNMR(DMSO-d₆): δ10.92(bs, 1H) 8.55(t, J= 6 and 5Hz, 1H), 8.14(s, 1H), 7.76(d, J=7 Hz, 1H), 7.68(m, 1H), 7.62(m, 1H), 7.45(m, 2H), 7.24(t, J=2.6Hz, 1H), 7.19(s, 1H), 7.15 (s, 1H), 7.10(m, 2H), 6.95(dd, J=1.5 and 8.7 Hz, 1H), 6.28(s, 1H), 3.04(t, J=6.8Hz, 2H), 1.82(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES− )454.3; (ES+)456.3 134m

—H —H 133m I-2 ¹HNMR(DMSO-d₆): δ13.30(bs, 1H), 8.62(t, J= 6 and 5Hz, 1H), 8.18(s, 1H), 7.87(d, J=7.9 Hz, 1H), 7.42(m, 3H), 7.09(m, 2H), 3.03(m, 1H), 3.1(t, J=6.8Hz, 2H), 1.86(m, 1H), 1.4 (m, 4H), 1.09(m, 1H), 0.89(d, J=6.8Hz, 6H); MS(ES−)421.2; (ES+)423.2 134n

—H —H 133n I-2 ¹HNMR(DMSO-d₆): δ15.89(bs, 1H), 8.56(t, J= 6 and 5Hz, 1H), 8.06(s, 1H), 7.67(m, 2H), 7.54(d, J=8.8Hz, 1H), 7.48(m, 4H), 7.05(m, 1H), 6.96(m, 2H), 3.77(s, 3H), 3.03(t, J=6.8 Hz, 2H), 1.81(m, 1H), 0.84(d, J=6.8Hz, 6 H); MS(ES−)502.3; (ES+)504.3 134o

—H —H 133o I-2 ¹HNMR(DMSO-d₆): δ13.07(bs, 1H), 8.63(t, J= 6 and 5Hz, 1H), 8.26(s, 1H), 8.05(d, J=4 Hz, 1H), 7.94(d, J=8Hz, 1H), 7.43(m, 5H), 7.28(m, 1H), 6.72(d, J=8.8Hz, 1H), 6.62(dd, J=5.5 and 6.5Hz, 1H), 3.34(m, 8H), 3.07(t, J= 6.8Hz, 2H), 1.82(m, 1H), 0.85(d, J=6.8 Hz, 6H); MS(ES−)486.3; (ES+)488.3 134p

—H —H 133p I-2 ¹HNMR(DMSO-d₆): δ12.94(bs, 1H), 10.20 (bs, 1H), 8.63(t, J=6 and 5Hz, 1H), 8.28(d, J= 1.5Hz, 1H), 7.96(m, 2H), 7.92(d, J=8.3 Hz, 1H), 7.68(m, 1H), 7.52(m, 2H), 7.4(m, 1 H), 7.3(m, 2H), 7.24(m, 1H), 3.08(t, J=6.8 Hz, 2H), 1.84(m, 1H), 0.88(d, J=6.8Hz, 6 H); MS(ES−)455.2; (ES+)479.2(M+Na) 134q

—H —H 133q I-2 ¹HNMR(DMSO-d₆): δ12.84(bs, 1H), 10.45 (bs, 1H), 8.62(t, J=6 and 5Hz, 1H), 8.27(d, J= , 1.5Hz, 1H), 8.01(s, 1H), 7.93(s, 2H), 7.9 (d, J=1.5Hz, 1H), 7.69(m, 1H), 7.57(d, J= 8.7Hz, 1H), 7.52(m, 2H), 7.29(d, J=8Hz, 1 H), 7.23(m, 1H), 7.02(dd, J=1.5 and 8.7Hz, 1 H), 3.07(t, J=6.8Hz, 2H), 1.83(m, 1H), 0.87 (d, J=6.8Hz, 6H), MS(ES−)455.2; (ES+) 479.3(M+Na) 134r

—H —H 133r I-2 ¹HNMR(DMSO-d₆): δ8.64(t, J=5.5Hz, 1H), 8.16(s, 1H), 7.87(d, J=7.1Hz, 1H), 7.50(m, 1 H), 7.40(d, J=4.1Hz, 2H), 7.19(b, 3H), 7.07 (m, 2H), 6.51(m, 2H), 6.35(d, J=7.8Hz, 2H), 3.97(d, J=5.6Hz, 2H), 3.13(t, J=6.5Hz, 2H), 1.90(m, 1H), 0.91(d, J=6.8Hz, 6H) 134s

—H —H 133s I-2 ¹HNMR(DMSO-d₆): δ9.53(bs, 1H), 8.67(t, J=4.7Hz, 1H), 8.32(s, 1H), 7.99 d, J=8.1Hz, 1 H), 7.70(d, J=7.6Hz, 1H), 7.52(m, 2H), 7.46 (d, J=11.5Hz, 1H), 7.32(m, 3H), 7.18(m, 3H), 4.33(s, 2H), 3.10(t, J=6.5Hz, 2H), 1.86(m, 1 H), 0.89(d, J=6.8Hz, 6H); MS(ES−)445.2 134t —OH —H —H 132 I-2 ¹HNMR(DMSO-d₆): δ12.57(b, 1H), 8.69(t, J=5.6Hz, 1H), 8.36(s, 1H), 7.99(d, J=7.9Hz, 1H), 7.92(d, J=7.7Hz, 1H), 7.57(t, J=7.5Hz, 1H), 7.46(t, J=7.7Hz, 1H), 7.23(d, J=5.2Hz, 1H), 7.17(d, J=7.5Hz, 1H), 3.12(t, J=6.5Hz, 2 H), 1.88(m, 1H), 0.91(d, J=6.8Hz, 6H); MS (ES−)340.2 134u

—H —H 133u I-2 ¹HNMR(DMSO-d₆): δ8.56(t, J=5.0Hz, 1H), 8.16(d, J=7.0Hz, 2H), 7.94(d, J=8.4Hz, 1H), 7.75(d, J=7.4Hz, 1H), 7.63(m, 2H), 7.46(m, 2 H), 7.21(b, 1H), 7.07(s, 2H), 6.99(t, J=5.1Hz, 1H), 3.05(t, J=6.5Hz, 2H), 1.83(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES−)416.3 134v

—H —H 133v I-2 ¹HNMR(DMSO-d₆): δ8.60(t, J=5.6Hz, 1H), 8.32(d, J=5.3Hz, 2H), 8.11(s, 1H), 7.78(d, J=7.7Hz, 1H), 7.65(d, J=5.5Hz, 1H), 7.55(m, 2H), 7.43(d, J=4.5Hz, 2H), 7.14(m, 3H), 3.06 (t, J=6.5Hz, 2H), 1.83(m, 1H), 0.86(d, J= 6.8Hz, 6H); MS(ES−)416.2 134w

—H —H 133w I-2 ¹HNMR(DMSO-d₆): δ10.10(bs, 1H), 9.31(s, 1 H), 8.65(t, J=5.7Hz, 1H), 8.27(s, 1H), 7.93(d, J=8.1Hz, 1H), 7.62(d, J=5.3Hz, 1H); 7.48(m, 2H), 7.28(s, 1H), 7.20(d, J=12.0Hz, 1H), 7.09 (s, 1H), 6.98(d, J=7.0Hz, 1H), 6.81(d, J=7.3 Hz, 1H), 6.37(t, J=7.6Hz, 1H), 3.09(t, J=6.5 Hz, 2H), 1.85(m, 1H), 0.90(d, J=6.8Hz, 6H); MS(ES−)431.1 134x

—H —H 133x I-2 ¹HNMR(DMSO-d₆): δ10.28(bs, 1H), 8.63(t, J=5.3Hz, 1H), 8.34(d, J=4.7Hz, 1H), 8.06(s, 1H), 7.82(d, J=6.6Hz, 1H), 7.53(m, 1H), 7.42 (m, 2H), 7.34(t, J=8.6Hz, 1H), 7.18(s, 1H), 7.07(d, J=2.7Hz, 2H), 6.10(b; 1H), 4.43(b; 1 H), 4.12(b, 1H), 3.12(t, J=6.5Hz, 2H), 1.89 (m, 1H), 0.90(d, J=6.8Hz, 6H); MS(ES+) 432.3, (ES−)430.2 134y

—H —H 133y I-2 ¹HNMR(DMSO-d₆): δ9.79(bs, 1H), 8.62(t, J=6.0Hz, 1H), 8.31(d, J=4.5Hz, 1H), 8.20(s, 1H), 8.08(s, 1H), 7.78(d, J=2.1Hz, 1H), 7.51 (m, 1H), 7.42(m, 2H), 7.06(m, 3H), 6.88(m, 1 H), 4.02(b, 2H), 3.13(t, J=6.5Hz, 2H), 1.90 (m, 1H), 0.93(d, J=6.8Hz, 6H); MS(ES+) 432.3, (ES−)430.3 134z

—H —H 133z I-2 ¹HNMR(DMSO-d₆): δ10.71(bs, 1H), 8.64(t, J=5.9Hz, 1H), 8.21(d, J=5.2Hz, 2H), 8.05(s, 1H), 7.81(d, J=7.7Hz, 1H), 7.51(m, 1H), 7.42 (m, 2H), 7.18(s, 1H), 7.04(t, J=1.4Hz, 2H), 6.51(b, 2H), 4.41(b, 1H), 4.01(b, 1H), 3.13(t, J=6.5Hz, 2H), 1.91(m, 1H), 0.91(d, J=6.8 Hz, 6H); MS(ES+)432.2, (ES−)430.2 134aa

—H —H 133aa I-2 ¹HNMR(DMSO-d₆): δ10.02(bs,  1H), 8.65(t, J=5.7Hz, 1H), 8.26(s, 1H), 7.94(d, J=7.7Hz, 1H), 7.66(d, J=5.8Hz, 1H), 7.51(m, 2H), 7.36 (d, J=8.4Hz, 2H), 7.29(d, J=7.9Hz, 1H), 7.22 (d, J=5.5Hz, 1H), 7.07(d, J=8.3Hz, 2H), 4.57 (t, J=9.0Hz, 1H), 3.51(m, 2H), 3.09(t, J=6.5 Hz, 2H), 2.62(t, J=6.6Hz, 2H), 1.85(m, 1H, 0.90(d, J=6.8Hz, 6H), MS(ES−)459.2 134ab

—H —H 133ab I-2 ¹HNMR(DMSO-d₆): δ9.05(s, 1H), 8.70(t, J=5.7Hz, 1H), 8.56(s, 1H), 8.36(s, 1H), 8.12 (m, 2H), 7.79(m, 1H), 7.60(m, 1H), 7.44(s, 2 H), 7.09(m, 2H), 6.56(d, J=8.9Hz, 1H), 4.89 (t, J=4.4Hz, 1H), 4.38(d, J=5.6Hz, 2H), 3.11 (t, J=6.5Hz, 2H), 1.84(m, 1H), 0.90(d, J= 6.8Hz, 6H), MS(ES−)461.1 134ac

—H —H 133ac I-2 ¹HNMR(DMSO-d₆): δ8.60(t, J=6 and 5Hz, 1 H), 8.13(s, 2H), 7.85(d, J=2Hz, 1H), 7.46 (m, 4H), 7.36(d, J=7.7Hz, 1H), 7.16(m, 4H), 7.10(m, 1H), 3.17(s, 3H), 3.08(t, J=6.8Hz, 2 H), 1.85(m, 1H), 0.89(d, J=6.8Hz, 6H), MS (ES−)469.2; (ES+)471.3 134ad

—H —H 133ad I-2 ¹HNMR(DMSO-d₆): δ8.55(t, J=6 and 5Hz, 1 H), 8.10(s, 2H), 7.73(d, J=7.2Hz, 1H), 7.54 (m, 4H), 7.46(m, 5H), 7.08(m, 3H), 3.04(t, J= 6.8Hz, 2H), 1.82(m, 1H), 0.86(d,J=6.8 Hz, 6H), MS(ES−)481.1; (ES+)483.3 134ae

—H —H 133ae I-2 ¹HNMR(DMSO-d₆): δ9.66(bs, 1H), 8.54(t, J= 6 and 5Hz, 1H), 8.12(s, 2H), 7.77(dd, J=8 and 2Hz, 1H), 7.6(dd, J=7 and 2Hz, 1H), 7.45(m, 5H), 7.10(m, 4H), 4.36(bs, 2H), 3.09 (t, J=6.8Hz, 2H), 1.86(m, 1H), 0.89(d, J= 6.8Hz, 6H), MS(ES−)469.2; (ES+)471.3 134af

—H —H 133af I-2 ¹HNMR(DMSO-d₆): δ9.76(s, 1H), 9.17(s, 1 H), 8.63(t, J=5.0Hz, 1H), 8.29(s, 1H), 7.90(d, J=1.6Hz, 1H), 7.60(s, 1H), 7.51(d, J=8Hz 1 H), 7.30(d, J=3.6Hz, 2H), 7.28(d, J=8.2Hz, 1 H), 7.22(t, 3H), 6.60(d, J=8.9Hz, 1H), 3.06(t, J=6Hz, 2H), 1.85(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES−)431.2 134ag

—H —H 133ag I-2 ¹HNMR(DMSO-d₆): δ9.64(s, 1H), 9.06(s, 1 H), 8.66(t, J=5.6Hz, 1H), 8.29(s, 1H), 7.95(d, J=7.9Hz, 1H), 7.63(m, 1H), 7.50(m, 2H), 7.29(d, J=3.1Hz, 1H), 7.20(d, J=8.9Hz, 1H), 7.11(m, 1H), 7.03(m, 1H), 6.60(d, J=8.9Hz, 1 H), 3.08(t, J=6Hz, 2H), 2.05(s, 3H), 1.85(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES−)445.2, MS(ES+)469.3(M+Na) 134ai

—H —H 133ai I-2, S MS(ES⁺): 472.2; MS(ES⁻): 470.2 135a

—CH═CH₂ —CH₃ 30f A-4 MS(ES⁺): 489.3 135b

—CH═CH₂ —CH₃ 30f A-4 MS(ES⁺): 475.3; MS(ES⁻): 473.3 135c

—CH═CH₂ —CH₃ 30f J MS(ES⁺): 573.5; MS(ES⁻): 571.3 135d

—CH═CH₂ —CH₃ 30f A-4 MS(ES⁻): 472.2 135e

—CH═CH₂ —CH₃ 30f J MS(ES⁻): 489.1 135f

—CH═CH₂ —CH₃ 30f J MS(ES⁻): 498.1 135g

—CH═CH₂ —CH₃ 30f J MS(ES⁻): 494.3 135h

—CH═CH₂ —CH₃ 30f J MS(ES⁻): 584.2 136a

—CH═CH₂ —H 135a I-2 ¹HNMR(DMSO-d₆): δ8.66(t, J=.55Hz, 1H), 8.35(t, J=4 and 6.4Hz, 1H), 8.28(d, J=2Hz, 1H), 7.95(dd, J=7.9 and 2Hz, 1H), 7.69(s, 1 H), 7.59(m, 2H), 7.25(d, J=8.1Hz, 2H), 7.15 (m, 2H), 6.93(s, 1H), 6.88(dd, J=17.7 and 11.5Hz, 1H), 5.95(d, J=17.7Hz, 1H), 5.37(d, J=11.5Hz, 1H), 3.76(t, J=6.8Hz, 2H), 3.10 (t, J=6.4Hz, 2H), 2.96(m, 2H), 1.86(m, 1H), 1.67(m, 2H), 0.89(d, J=6.8Hz, 6H); MS # (ES−)473.3; (ES+)475.3 136b

—CH═CH₂ —H 135b I-2 ¹HNMR(DMSO-d₆): δ8.64(t, 1H), 8.51(s, 1 H), 8.21(s, 1H), 7.88(d, J=7.8Hz, 1H), 7.74(s, 1H), 7.56(s, 2H), 7.15(m, 2H), 6.80(t, 2H), 5.90(d, J=17Hz, 1H), 5.36(d, J=11.0Hz, 1H), 3.18(m, 2H), 3.06(t, J=6Hz, 2H), 2.43(m, 2 H), 1.85(m, 1H), 0.86(d, J=6.8Hz, 6H); MS (ES+)461.2, MS(ES−)459.2 136c

—CH═CH₂ —H 135c I-2, S ¹HNMR(DMSO-d₆/D₂O): δ8.71(t, 1H), 8.27 (d, J=3Hz, 1H), 8.21(d, J=3Hz, 1H), 7.96(q, 1 H), 7.79(q, 1H), 7.72(s, 1H), 7.63(d, J=8Hz 1 H), 7.30(d, J=6Hz, 1H), 7.24(d, J=7Hz, 1H), 6.87(q, 2H), 6.00(d, J=8Hz, 1H), 5.41(d, J=8 Hz, 1H), 3.06(t, J =6Hz, 2H), 1.85(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES+)459.2 136d

—CH═CH₂ —H 135d I-2 ¹HNMR(DMSO-d₆): δ12.86(bs, 1H), 9.17(s, 1 H), 8.65(t, J=6Hz, 1H), 8.29(d, J=2Hz, 1 H), 8.26(s, 2H), 7.97(dd, J=8 and 2Hz, 1H), 7.76(s, 1H), 7.63(d, 8Hz, 1H), 7.31(d, J=8 Hz, 1H), 7.24(d, J=8Hz, 1H), 6.86(dd, J= 10.7 and 17.5Hz, 1H), 6.49(s, 1H), 5.99(d, J= 17.5, 1H), 5.40(d, J=10.7Hz, 1H), 3.10(t, J= 6.8Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.8Hz, 6 H); MS(ES−)458.2, (ES+)460.3 136e

—CH═CH₂ —H 135e I-2 ¹HNMR(DMSO-d₆): δ12.72(s, broad, 1H), 8.65(t, J=5.7Hz, 1H), 8.29(s, 1H), 7.93(d, J=7.9Hz, 1H), 7.74(m, 2H), 7.65(d, J=6Hz 1 H), 7.42(d, J=7.9Hz, 1H), 7.24(m, 3H), 7.11 (m, 1H), 6.84(q, J=11.1, 17.8Hz, 1H), 5.97(d, J=18Hz, 1H), 5.58(d, 1H), 5.41(d, 1H), 3.08 (t, J=6Hz, 2H), 1.85(m, 1H), 0.86(d, J=6.8 Hz, 6H); MS(ES−)475.1 136f

—CH═CH₂ —H 135f I-2 ¹HNMR(DMSO-d₆): δ8.67(t, J=6.06Hz, 1H), 8.28(s, 1H), 7.90(d, J=7.7Hz, 1H), 7.67(m, 4 H), 7.32(m, 5H), 7.09(d, J=7.9Hz 1H), 6.89 (q, J=10.9 & 18.0Hz, 1H), 5.99(d, J=17.5Hz, 1 H), 5.42(d, J=11Hz, 1H), 3.08(t, J=6.3Hz, 2 H), 1.88(m, 1H), 0.87(d, J=6.8Hz, 6H); MS (ES−)484.2 136g

—CH═CH₂ —H 135g I-2 ¹HNMR(DMSO-d₆): δ10.38(s, 1H), 8.66(t, J=6.06Hz, 1H), 8.29(s, 1H), 7.95(d, J=6.1Hz, 1H), 7.75(s, 1H), 7.63(d, 2H), 7.43(d, 2H), 7.26(m, 3H), 7.00(d, J=7.7Hz, 1H), 6.85(q, J=10.9 & 18.0Hz, 1H), 5.98(d, J=17.5Hz, 1H), 5.40(d, J=11Hz, 1H), 3.98(s, 2H), 3.08(t, J=6.3Hz, 2H), 1.86(m, 1H), 0.88(d, J=6.8 Hz, 6H); MS(ES−)480.2 136h

—CH═CH₂ —H 135h S, I-2 ¹HNMR(DMSO-d₆): δ8.55(t, J=6.06Hz, 1H), 8.02(s, 1H), 7.60(m, 4H), 7.21(t, J=7.1, 2H), 6.99(m, 2H), 6.83(d, J=6.8Hz, 1H), 6.81(q, J=10.9 & 18.0Hz, 1H), 5.92(d, J=17.5Hz, 1H), 5.35(d, J=11Hz, 1H), 3.89(s, 2H), 3.03(t, J=6.3Hz, 2H), 1.36(m, 1H), 0.86(d, J=6.8 Hz, 6H)

Cpd. Starting Method No. —R′ —R″ R′″ X From Used Analytical Data 117n —OBn —CHO —CH₃ N 116 + D-2 MS(ES⁺): 477.2 220a 118n —OBn —CO₂H —CH₃ N 117n E Characterized at the next step 119n —OBn —CO₂MEM —CH₃ N 118n F Characterized at the next step 120n —OH —CO₂MEM —CH₃ N 119n G Characterized at the next step 121n —OSO₂CF₃ —CO₂MEM —CH₃ N 120n B-2 Characterized at the next step 122n —CH═CH₂ —CO₂MEM —CH₃ N 121n D-3 Characterized at the next step 123n —CH═CH₂ CO₂H —CH₃ N 122n I-1 MS(ES⁻): 411.1 124n —CH═CH₂

—CH₃ N 123n J MS(ES⁺): 530.3 125n —CH═CH₂

H N 124n I-2 1H NMR(DMSO-d6 + H2O): 8.24(d, J=7.7Hz, 1H), 8.0-7.9(m, 2H), 7.81(s, 4H), 7.14-6.94(m, 2H), 6.08(d, J=17.3Hz, 1H), 5.48(d, J=12.05Hz, 1H), 3.87(s, 3H), 3.20(d, J=6.4Hz, 2H), 2.04-1.75(1H, m), 0.92(d, J=6.4Hz, 6H). MS(ES+): 516.34. 189f —OH —CHO —CH₃ CH 117a AL MS(ES⁺): 386.4. 189g —OH —CHO —CH₃ N 117n AL MS(ES⁺): 387.38 189h —OSO₂CF₃ —CHO —CH₃ CH 189f B-2 MS(ES⁺): 518.2 189i —OSO₂CF₃ —CHO —CH₃ N 189g B-2 MS(ES⁺): 541.1( M + Na) 189j —CH═CH₂ —CHO —CH₃ CH 189h D-3 MS(ES⁺): 418.3 (M + Na) 189k —CH═CH₂ —CHO —CH₃ N 189i D-3 MS(ES⁺): 397.3 189l —CH═CH₂

H CH 189j AE-3 ¹H NMR(DMSO-d₆): δ 8.63(t, J=5Hz, 1H), 8.56(bs, 4H), 8.33(s, 1H), 7.90(d, J=8Hz, 1H), 7.61(m, 1H), 7.50(s, 1H), 7.47(2, 1H), 7.41(s, 1H), 7.30(d, J=7.2Hz, 1H), 6.94(dd, J=11 & 17.5Hz, 1H), 6.67(m, 3H), 5.62(d, J=17.5Hz, 1H), 5.20(d, J=11Hz, 1H), 4.01(m, 2H), 3.73(s, 3H), 3.09(t, J=6.5Hz, 2H), # 1.86(m, 1H), 0.80(d, J=6.5Hz, 6H); MS(ES⁺) 501.46 189m —CH═CH₂

H N 189k AE-3 ¹H NMR(DMSOd6 + H2O): 8.20(d, J=7.9Hz, 1H), 8.04(d, J=7.9Hz, 1H), 7.67-7.45(m, 4H), 6.94(dd, J=17.3 and 11.1Hz, 1H), 6.5(d, J=8.3Hz, 1H), 5.73(d, J=17.9Hz, 1H), 5.28(d, J=11.3Hz, 1H), 4.01(s, 2H), 3.76(s, 3H), 3.18 (d, J=6.9Hz, 2H), 2.0-1.76(m, 1H), 0.91(d, J=6.6Hz, 6H); MS(ES+): 502.34 189n —CH═CH₂

H CH 189j AE-3 ¹H NMR [DMSO/DCl (1 drop)]: δ 8.34(m, 3H), 8.3(d, J=8.3Hz, 1H), 8.02(d, J=7.7Hz, 1H), 7.69(bs, 1H), 7.43(d, J=8Hz, 1H), 6.98(dd, J=11 & 17Hz, 1H), 6.75(s, 1H), 5.88(d, J=17Hz, 1H), 5.32(d, J=11Hz, 1H), 4.40(m, 2H), 3.77(s, 3H), 3.09(d, J=7Hz), 1.87(m, 1H), 0.89(d, J=7Hz, 6H); MS(ES⁺) 502.39

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 148a

—CH₃

147a J ¹H NMR (DMSO-d₆): δ 10.65(s, 1H), 10.15(s, 1H), 9.19(s, 2H), 8.88(s, 2H), 8.10(d, J=2.1Hz, 1H), 7.92(s, 1H), 7.93-7.75(m, 6H), 7.31(dd, J=8.4 and 23.9Hz, 1H), 7.12(d, J=3.5Hz, 1H), 6.67(m, 1H), 3.53(s, 3H), 2.20(d, J=7.0Hz, 2H), 2.07(m, 1H), 0.94(d, J=6.3Hz, 6H). 148b

—CH₃

147b J ¹H NMR(DMSO-d₆): δ 10.65(s, 1H), 10.09(s, 1H), 9.17(s, 1H), 8.83(s, 1H), 8.10(d, J=2.0Hz, 1H), 7.85(d, J=2.0Hz, 2H), 7.81(d, J=2.0 and 7.9Hz, 2H), 7.76(m, 5H), 7.66(d, J=3.9Hz, 1H), 7.62(d, J=4.9Hz, 1H), 7.31(d, J=7.9Hz, 1H), 7.26(d, J=7.9Hz, 1H), 7.19(t, J=3.9Hz, 1H), 3.53(s, 1H), 2.19(d, J=6.9Hz, 2H), 2.06(m, # J=6.9Hz, 1H), 0.92(d, J=6.9Hz, 6H); MS(ES⁺): 555.67 148c —CH═CH₂ —CH₃

147c J Characterized in the next step 149a

—H

148a I-2 MS(ES⁺): 525.3 149b

—H

148b I-2 ¹H NMR(DMSO-d₆): δ 13.95(s, 1H), 9.79(s, 1H), 8.87(s, 4H), 7.76(s, 1H), 7.65(m, 8H), 7.46(dd, J=2.1 and 8.4Hz, 1H), 7.16(t, J=4.2Hz, 1H), 7.04(d, J=7.7Hz, 1H), 6.76(d, J=8.4Hz, 1H), 2.13(d, J=7.0Hz, 2H), 2.03(m, J=6.3 and 7.0Hz, 1H), 0.90(d, J=6.3Hz, 6H); MS(ES⁺): 541.62 149c —CH═CH₂ —H

148c I-2 MS(ES⁺): 485.6 175 —H —CH₃

174 J ¹H NMR(DMSO-d₆): δ 8.81(m, 4H), 8.37(t, J=6.0Hz, 1H), 7.74-7.23(m, 11H), 4.31(d, J=6.2Hz, 2H), 3.51(s, 3H), 2.44(m, 1H), 1.04(d, J=7.0Hz, 6H); MS(ES⁺): 473.3 176 —H —H

175 I-2 ¹H NMR(DMSO-d₆): δ 13.79(br s, 1H), 9.03(m, 3H), 8.25(m, 1H), 7.78-7.35(m, 7H), 6.99(m, 2H), 6.79(m, 1H), 4.20(br s, 2H), 3.51(s, 3H), 2.39(m, 1H), 1.00(d, J=6.8Hz, 6H); MS(ES⁺): 459.3 182 —H —CH₃

178 J ¹H NMR(DMSO-d₆): δ 8.96(m, 2H), 7.79-7.38(m, 9H), 7.29(dd, J=7.5 and 1.7Hz, 2H), 4.42(s, 2H), 3.50(s, 3H), 2.97(s, 2H), 1.87(m, 1H), 1.36(m, 9H), 0.81(d, J=6.8Hz, 6H); MS(ES⁺): 559.5 183 —H —H

182 I-2, S ¹H NMR(DMSO-d₆): δ 9.11(m, 4H), 7.86(s, 1H), 7.66(m, 5H), 7.49(m, 2H), 7.38(m, 1H), 7.08(m, 2H), 4.12(s, 2H), 2.59(m, 2H), 1.87(m, 1H), 0.81(d, J=6.6Hz, 6H); MS(ES⁺): 445.32

N (in Ring With Cpd. Respect to Starting Method No. Phenyl) —R —R′ From Used Analytical Data 151 3 —CHO —CH₃ 150 + D-9 MS(ES⁻): 339.3  3a 152 3 —CO₂H —CH₃ 151 E ¹H NMR(CDCl₃): δ 8.69(t, J=5.8Hz, 1H), 8.50(d, J=4.9Hz, 1H), 8.33(d, J=1.7Hz, 1H), 8.24(s, 1H), 8.01(dd, J=7.9, 1.9Hz, 1H), 7.53(d, J=5.1Hz, 1H), 7.34(d, J=8.1Hz, 1H), 3.56(s, 3H), 3.12(m, 2H), 1.87(m, 1H), 0.91(d, J=6.6Hz, 6H) 153 3

—CH₃ 152 J ¹H NMR(CD₃OD): δ 8.75(d, J=4.7Hz, 2H), 8.55(s, 1H), 8.42(d, J=1.9Hz, 1H), 8.07(dd, J=8.1, 1.9, 1H), 7.74(s, 3H), 7.70(d, J=5.1Hz, 1H), 7.51(d, J=8.1Hz, 1H), 3.69(s, 3H), 3.21(m, 2H), 1.94(m, 1H), 0.98(d, J=6.6Hz, 6H); MS(ES⁺): 474 154 3

—H 153 I-2 ¹H NMR(DMSO): δ 11.18(s, 1H), 9.31(s, 2H), 9.10(s, 2H), 8.92(d, J=5.1Hz, 1H), 8.78(m, 2H), 8.43(d, J=1.5Hz, 1H), 8.07(dd, J=7.9, 1.3Hz, 1H), 7.97(d, J=5.3Hz, 1H), 7.82(d, J=8.7Hz, 2H), 7.72(d, J=8.8Hz, 2H), 7.50(d, J=7.9Hz, 1H), 3.10(t, J=6.0Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.6Hz, 6H); MS(ES⁺) 460 156 4 —CHO —CH₃ 155 + D-9 MS(ES⁺): 341.4  3a 157 4 —CO₂H —CH₃ 156 E ¹H NMR(CDCl₃): δ 8.80(s, 1H), 8.46(d, J=5.1Hz, 1H), 8.29(s, 1H), 7.85(d, J=7.9Hz, 1H), 7.13(d, J=7.9Hz, 1H), 7.00(d, J=5.1Hz, 1H), 6.83(bs, 2H), 3.45(s, 3H), 3.15(m, 2H), 1.84(m, 1H), 0.90(d, J=6.6Hz, 6H); MS(ES⁻): 355.2 158 4

—CH₃ 157 J ¹H NMR(CD₃OD): δ 8.85(s, 1H), 8.75(d, J=5.3Hz, 1H), 8.41(d, J=1.9Hz, 1H), 8.07(dd, J=8.1, 2.1, 1H), 7.74(s, 4H), 7.48(d, J=8.1Hz, 1H), 7.45(d, J=5.1Hz, 1H), 3.69(s, 3H), 3.21(m, 2H), 1.94(m, 1H), 0.97(d, J=6.8Hz, 6H); MS(ES⁻): 472.4 159 4

—H 158 I-2 ¹H NMR(DMSO): δ 10.97(s, 1H), 9.24(s, 2H), 8.96(s, 3H), 8.79(m, 2H), 8.40(d, J=1.8Hz, 1H), 8.06(d, J=7.7Hz, 1H), 7.77(s, 4H), 7.52(m, 1H), 7.38(d, J=7.5Hz, 1H), 3.10(m, 2H), 1.85(m, 1H), 0.89(d, J=5.3, 6H); MS(ES⁺) 460.2

Cpd. Starting Method No. —R —R′ From Used Analytical Data 161a —CH₃ —CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ 10.55(s, 1H), 9.00(bs, 2H), 8.68(t, J= 5.8Hz, 1H), 8.24 (d, J= 1.9Hz, 1H), 8.04(d, J= 8.1Hz, 1H), 7.91(d, J= 8.8Hz, 2H), 7.77(d, J= 1.3Hz, 1H), 7.67(m, 3H), 7.40(d, J= 7.9Hz, 1H), 7.29(d, J= 7.9Hz, 1H), 6.90(dd, J= 17.7, 11.0Hz, 1H), 6.03(d, J= 17.7Hz, 1H), 5.42(d, J= 11.0Hz, 1H), 3.61(s, 3H), 3.56(s, 3H), 3.10(t, J= 6.4Hz, 2H), 1.85(m, 1H), 0.90(d, J= 6.5Hz, 6H); MS (ES+): 557.3 161b —C₂H₅ —CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ 10.54(s, 1H), 9.20(bs, 4H), 8.67(t, J= 6Hz, 1H), 8.24(1H), 8.02(1H), 7.91(2H), 7.77(1H), 7.66(m, 3H), 7.40(1H), 7.29(1H), 6.88(dd, J= 17.3, 10.7Hz, 1H), 6.03(d, J= 17.3Hz, 1H), 5.42(d, J= 10.7Hz, 1H), 3.56(s, 3H), 3.5(m, 3H), 3.09(2H), 1.85(m, 1H), 0.89(6H); MS (ES+): 571.3 161c —CH₂C₆H₅ —CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ 10.54(s, 1H), 9.20(bs, 2H), 8.68(t, J= 5.8Hz, 1H), 8.24(d, J= 1.9Hz, 1H), 8.03(d, J= 8.1Hz, 1H), 7.92(d, J= 8.8Hz, 2H), 7.77(s, 1H), 7.68(m, 4H), 7.36(m, 6H), 6.89(dd, J= 17.7, 11.2Hz, 1H), 5.05(s, 2H), 6.03(d, J= 17.7Hz, 1H), 5.42(d, J= 11.2Hz, 1H), 3.56(s, 3H), 3.09(t, J= 6.6Hz, 2H), 1.84(m, 1H), 0.89 (d, J= 6.6Hz, 6H); MS (ES+): 633.3 161d —C(CH₃)₃ —CH₃ 31f AB-2 MS (ES⁺): 599.3 and 499.3 161e —CH₂—CCl₃ —CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ □ 10.59(s, 1H), 9.24(s, 2H), 8.68(t, J= 5.6Hz, 1H), 8.24 (d, J= 1.8Hz, 1H), 8.03(dd, J= 8.9, 1.9Hz, 1H), 7.96(d, J= 8.9Hz, 2H), 7.79(d, J= 1.5Hz, 1H), 7.69(m, 3H), 7.41(d, J= 8.1Hz, 1H), 7.29(d, J= 8.0Hz, 1H), 6.89(dd, J= 17.7, 11.1Hz, 1H), 6.03(d, J= 17.7Hz, 1H), 5.42(d, J= 11.1Hz, 1H), 4.88(s, 2H), 3.56 (s, 3H), 3.10(t, J= 6.6Hz, 2H), 1.85(m, 1H), 0.89(d, J= 6.6Hz, 6H); MS (ES+): 674.97 161f

—CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ □ 10.58(s, 1H), 9.15(s, 2H), 8.69(t, J= 5.4Hz, 1H), 8.25(d, J= 1.8Hz, 1H), 8.04(dd, J= 8.1, 1.9Hz, 1H), 7.95(d, J= 8.9Hz, 2H), 7.78(s, 1H), 7.68 (m, 3H), 7.40(d, J= 8.0Hz, 1H), 7.29(d, J= 8.0Hz, 1H), 7.07(d, J= 8.8Hz, 2H), 6.93 (d, J= 8.8Hz, 2H), 6.89(dd, J= 17.7, 11.1Hz, 1H), 6.03(d, J= 17.7Hz, 1H), 5.42(d, J= 11.1Hz, 1H), 3.75(s, 3H), 3.57(t, J= 6.6Hz, # 2H), 1.85(m, 1H), 0.89 (d, J= 6.6Hz, 6H); MS (ES+): 649.3 161g

—CH₃ 31f AB-2 ¹H NMR (DMSO-d6): δ 10.59(s, 1H), 9.19(s, 2H), 8.68(t, J= 5.7Hz, 1H), 8.25(d, J= 1.8Hz, 1H), 8.03(dd, J= 8.1, 1.9Hz, 1H), 7.95(d, J= 8.9Hz, 2H), 7.78(d, J= 1.7Hz, 1H), 7.70(m, 3H), 7.41(d, J= 8.1Hz, 1H), 7.29(d, J= 7.9Hz, 1H), 7.20(m, 4H), 6.90 (dd, J= 17.9, 11.1Hz, 1H), 6.03(d, J= 17.9Hz, 1H), 5.42(d, J= 11.1Hz, 1H), 3.57(s, 3H), 3.10(t, J= 6.8Hz, 2H), 1.85(m, 1H), 0.89(d, J= #6.6Hz, 6H); MS (ES+): 637.5 161h

—CH₃ 31f AB-1 ¹H NMR (DMSO-d6): δ 10.58(s, 1H), 9.00(bs, 2H), 8.68(t, J= 5.9Hz, 1H), 8.24(d, J= 1.9Hz, 1H), 8.03(d, J= 8.1Hz, 1H), 7.94(d, J= 8.9Hz, 2H), 7.78(d, J= 1.5Hz, 1H), 7.68(m, 3H), 7.40(d, J= 8.1Hz, 1H), 7.29(d, J= 8.1Hz, 1H), 6.89(dd, J= 17.5, 11.0Hz, 1H), 6.03(d, J= 17.5Hz, 1H), 5.71(s, 2H), 5.42(d, J= 11.0Hz, 1H), 3.56(s, 3H), 3.10 (t, J= 6.2Hz, 2H), 2.07(s, 3H), 1.85(m, 1H), 0.89(d, J= #6.6Hz, 6H); MS (ES+): 615.3 161i

—CH₃ 31f AB-1 ¹H NMR (DMSO-d6): δ 10.57(s, 1H), 9.22(s, 2H), 8.67(t, J= 5.9Hz, 1H), 8.24(d, J= 1.9Hz, 1H), 8.03(dd, J= 8.1, 1.9Hz, 1H), 7.94(d, J= 8.9Hz, 2H), 7.78(d, J= 1.5Hz, 1H), 7.69(m, 3H), 7.41(d, J= 7.9Hz, 1H), 7.29(d, J= 7.9Hz, 1H), 6.89(dd, J= 17.7, 11.1Hz, 1H), 6.03(d, J= 17.7Hz, 1H), 5.73(s, 2H), 5.42(d, J= 11.1Hz, 1H), 3.56(s, 3H), 3.09(t, J= 6.6Hz, 2H), 1.85(m, 1H), 1.14(s, 9H), 0.89 #(d, J= 6.7Hz, 6H); MS (ES+): 657.52 161j

—CH₃ 31f AB-1 ¹H NMR (DMSO-d6): δ □ 10.57(s, 1H), 9.24(s, 1H), 9.17(s, 1H), 8.68(t, J= 6.2Hz, 1H), 8.25(s, 1H), 8.04(d, J= 8.2Hz, 1H), 7.94(d, J= 7.5Hz, 2H), 7.67(s, 1H), 7.67 (m, 3H), 7.40(d, J= 7.9Hz, 1H), 7.29(d, J= 7.9Hz, 1H), 6.90(dd, J= 17.8, 11.1Hz, 1H), 6.71(q, J= 5.5Hz, 1H), 6.03(d, J= 17.7Hz, 1H), 5.42(d, J= 11.1Hz, 1H), 3.56(s, 3H), 3.10(t, J= 6.6Hz, 2H), 2.00(s, 3H), 1.85(m, 1H), 1.43 #(d, J= 5.5Hz, 3H), 0.89(d, J= 6.7Hz, 6H); MS (ES+): 629.4 162a —CH₃ —H 161a I-2 ¹H NMR (DMSO-d6): δ 9.04(bs, 3H), 8.57(t, J= 5.4Hz, 1H), 8.16(s, 1H), 7.86(d, J= 8.5Hz, 2H), 7.79(d, J= 7.9Hz, 1H), 7.72(s, 1H), 7.58(m, 3H), 7.12(d, J= 8.0Hz, 2H), 6.87(dd, J= 17.7, 11.0Hz, 1H), 5.97(d, J= 17.7Hz, 1H), 5.37(d, J= 11.0Hz, 1H), 3.59 (s, 3H), 3.05(t, J= 6.6Hz, 2H), 1.83(m, 1H), 0.87(d, J= 6.6Hz, 6H); MS (ES+): 543.38 162b —C₂H₅ —H 161b I-2 ¹H NMR (DMSO-d6): δ 12.8(bs, 1H), 10.8(bs, 1H), 9.20(bs, 2H), 8.68(t, J= 5.9Hz, 1H), 8.24(d, J= 1.9Hz, 1H), 7.91(m, 3H), 7.77(d, J= 1.5Hz, 1H), 7.64(m, 3H), 7.28 (d, J= 8.1Hz, 1H), 7.22(d, J= 8.1Hz, 1H), 6.87(dd, J= 17.7, 11.4Hz, 1H), 6.01(d, J= 17.7Hz, 1H), 5.42(d, J= 11.4Hz, 1H), 4.05(q, J= 7.2Hz, 2H), 3.08(t, J= 6.4Hz, 2H), 1.84(m, 1H), 1.21(t, J= 7.2Hz, 3H), 0.88(d, J= 6.6Hz, 6H); MS (ES⁻): 555.2 162c —CH₂C₆H₅ —H 161c I-2 ¹H NMR (DMSO-d6): δ 12.7(bs, 1H), 10.75(bs, 1H), 9.15(b, 2H), 8.63(t, J= 5.8Hz, 1H), 8.27(bs, 1H), 7.90(d, J= 8.3Hz, 2H), 7.77(s, 1H), 7.43-7.15(m, 8H), 7.40(d, J= 8.1Hz, 1H), 7.29(d, J= 8.1Hz, 1H), 6.87(dd, J= 17.4, 11.0Hz, 1H), 6.03(d, J= 17.5Hz, 1H), 5.71(s, 2H), 5.42(d, J= 11.0Hz, 1H), 5.09(s, 2H), 3.08(t, J= 6.4Hz, 2H), 1.85(m, 1H), 0.88(d, J= 6.6Hz, 6H); MS (ES+1): 619.2 162d —C(CH₃)₃ —H 161d I-2 ¹H NMR (DMSO-d6): δ 12.6(bs, 1H), 11.0(bs, 1H), 9.04(b, 2H), 8.62(t, J= 5.4Hz, 1H), 8.24(s, 1H), 7.86(m, 3H), 7.77(s, 1H), 7.62(m, 3H), 7.24(d, J= 8.2Hz, 1H), 7.20(d, J= 8.0Hz, 1H), 6.87(dd, J= 17.2, 11.0Hz, 1H), 6.00(d, J= 17.7Hz, 1H), 5.40 (d, J= 11.0Hz, 1H), 3.07(t, J= 6.3Hz, 2H), 1.84(m, 1H), 1.44(s, 9H), 0.88(d, J= 6.6Hz, 6H); MS (ES+1): 585.4

Cpd. Starting Method No. —R —R′ From Used Analytical Data 164 —CHO —CH₃ 163 + 130 D-2 ¹HNMR (DMSO-d₆): δ 9.58(s, 1H), 7.91(dd, J= 1.2, 8.0Hz, 1H), 7.71(dt, J= 1.2 and 7.4Hz, 1H), 7.58(t, J= 7.4Hz, 1H), 7.41(m, 2H), 7.38(m, 1H), 7.32(d, J= 8Hz, 1H), 7.24(d, J= 7.4Hz, 1H), 3.52(q, J= 16 and 26Hz, 2H), 3.35(s, 3H); MS (ES+): 255.32 165 —CO₂H —CH₃ 164 E Characterized in the next step 166

—CH₃ 165 J ¹HNMR (DMSO-d₆): δ 10.34(s, 1H), 9.18(s, 2H), 8.92(s, 2H), 7.72-7.5(m, 7H), 7.34-7.14(m, 5H), 3.60(q, J= 17 & 40Hz, 2H), 3.48(s, 3H); MS (ES+) 388.67 167

—H 166 I-2 ¹HNMR (DMSO-d₆): δ 11.74(bs, 1H), 9.90(s, 1H), 8.79(bs, 2H), 7.64(m, 1H), 7.50(m, 7H), 7.33(d, J= 8.6Hz, 1H), 7.26(d, J= 7.4Hz, 1H), 7.12(t, J= 7.4Hz, 1H), 7.02(t, J= 7.4Hz, 1H), 6.89(d, J= 6.8Hz, 1H), 3.83(d, J= 15Hz, 2H); MS (ES+) 374.79

Cpd. Starting Method No. —R —R′ —R″ —R′″ From Used Analytical Data 188a —CH═CH₂ 4)

—H 187a AE-3 MS (ES⁺): 485.4(100% M⁺¹) 188b —CH═CH₂ 4)

—H 187b AE-3 ¹HNMR (DMSO-d₆/D₂O): δ 8.5(d, J= 2Hz, 1H), 8.17(dd, J= 8Hz, 2H), 7.65(s, 1H), 7.63(s, 1H), 7.54(d, J= 8Hz, 1H), 7.49(bs, 2H), 7.14(d, J= 7.7Hz, 1H), 6.78(dd, J= 11 and 17Hz, 1H), 6.62(d, J= 9hz, 1H), 5.83(d, J= 17hz, 1H), 5.33 (d, J= 11hz, 1H), 4.17(d, J= 9hz, 1H), 4.12(s, 2H); MS (ES+): 497.3 188c —CH═CH₂ 4)

—H 187c AE-3 ¹HNMR (DMSO-d₆/D₂O): δ 8.6(m, 3H), 8.3(m, 3H), 7.9(d, J= 7.9Hz, 1H), 7.45(d, J= 8.8Hz, 1H), 7.3(m, 3H), 7.1(m, 1H), 7.0 (d, J= 8.1Hz, 1H), 6.6(dd, J= 6 and 28Hz, 1H), 6.4(d, J= 8.8Hz, 2H), 5.7(d, J= 17Hz, 1H), 5.15(d, J= 11Hz, 1H), 3.9(m, 2H), 3.25(m, 2H), 1.1(t, J= & Hz, 3H); MS (ES+): 443.3 188d —CH═CH₂ 4)

H 187d AE-3 ¹HNMR (DMSO-d₆): δ 8.8(m, 2H), 8.7(m, 1H), 8.4(m, 2H), 8.1(m, 1H), 7.6(m, 2H), 7.5(m, 3H), 7.3(m, 1H), 7.2(m, 1H), 6.8 (m, 1H), 6.6(m, 2H), 5.8(m, 1H), 5.3(m, 1H), 4.1(m, 2H), 3.31(m, 1H), 3.2(m, 1H), 1.7(m, 1H), 1.6(m, 1H), 1.3(m, 1H), 1.0 (m, 6H); MS (ES+): 485 189a —OCH₃ 3)

—H 74 AE-4, I-2 ¹HNMR (DMSO-d₆): δ 8.60(t, J= 6Hz, 1H), 8.39(bs, 2H), 8.28(bs, 1H), 7.78(m, 1H), 7.56(m, 1H), 7.43(dd, J= 5.8Hz, 3.8Hz, 2H), 7.18(m, 2H), 6.80(m, 3H), 6.51(bs, 1H), 4.10(m, 1H), 3.85(m, 1H), 3.70(s, 3H), 3.17(t, J= 6Hz, 2H), 1.80(m, 1H), 0.89(d, J= 6.8Hz, 6H); MS (ES⁺) 475.2 189b —OBn (4)

—H 184a AE-3 ¹HNMR (DMSO-d₆/D₂O): δ 8.24(d, J= 1.5Hz, 1H), 7.86(d, J= 7Hz, 1H), 7.49(m, 2H), 7.36(m, 4H), 7.26(d, J= 8.3Hz, 1H), 6.94(m, 3H), 6.66(d, J= 8.7Hz, 2Hz, 2H), 5.03(s, 2H), 4.06(q, J= 16 and 21Hz, 2H), 3.02(d, J= 7Hz, 2H), 1.86(m, 1H), 0.89(d, J= 6.8Hz, 6H); MS (ES−): 549.2 and (ES⁺) 551.4 189c —OH (4)

—H 189b G ¹HNMR (DMSO-d₆): δ 11.3(bs, 1H), 9.07(s, 1H), 8.46(t, J= 6Hz, 1H), 8.27(bs, 2H), 8.15(bs, 2H), 7.66(d, J= 7.7Hz, 1H), 7.36(d, J= 8.5Hz, 2H), 7.03(d, J= 8.1Hz, 1H), 6.77(m, 2H), 6.68(d, J= 8.3Hz, 2Hz, 2H), 6.6(s, 1H), 6.47 9d, J= 8.2Hz, 1H), 4.05(d, J= 14Hz, 1H), 3.09(d, J= 14Hz, 1H), 3.01(t, J= 7Hz, 2H), 1.79(m, 1H), 0.82(d, J= 6.8Hz, 6H); MS (ES−): # 459.2 and(ES⁺) 461.4 189d —H

—H 131 AE-3 MS (ES⁺): 445.4; MS (ES⁻): 443.3 189e —H

—H 131 AE-3 MS (ES⁺): 446.46; MS (ES⁻): 444.45

Cpd. Starting Method No. —R —R′ From Used Analytical Data 205

—Boc 204 A-4 ¹HNMR (DMSO-d₆): δ 11.04(s, 0.6H), 10.97(bs, 0.4H), 8.66(t, J= 5.6Hz, 0.6H), 8.56(t, J= 5.6Hz, 0.4H), 8.22(s, 1H), 8.11(d, J= 2Hz, 0.6H), 8.03(d, J= 2Hz, 0.4H), 7.94(dd, J= 2 and 8Hz, 1H), 7.82(m, 4H), 7.40(m, 8H), 7.18(m, 2H), 7.04(m, 2H), 5.21(s, 0.8H), 5.11(s, 1.2H), 3.11(t, J= 6.2Hz, 1.2H), 3.06(t, J= 6.2Hz, 0.8H), 1.84(m, 1H), 1.43(s, 5.4H), 1.42(s, 3.6H), 0.91(d, J= 6.8Hz, 3.6H), 0.88 #(d, J= 6.8Hz, 2.4H); MS (ES+): 665.5 206 —CH₂OH —Boc 204 A-6 ¹HNMR (DMSO-d₆): δ 12.15(bs, 1H), 11.07(bs, 1H), 10.69(s, 1H), 10.38(bs, 1H), 8.68(t, J= 5.6Hz, 1H), 8.12(d, J= 1.7Hz, 1H), 8.00(dd, 1.8, 8Hz, 1H), 7.68(m, 4H), 7.46-7.30(m, 6H), 7.16 (d, J= 2.8Hz, 1H), 7.01(d, J= 8.5Hz, 1H), 6.86(dd, J= 8.5 and 2.8Hz, 1H), 5.07(s, 2H), 4.30(d, J= 7.4Hz, 2H), 3.15(t, J= 6.2Hz, 2H), 1.86(m, 1H), 1.53(s, 9H), 0.89(d, J= 6.8Hz, 6H); MS (ES−): 649.4 207 —CH₂OH —H 206 S-2 ¹HNMR (DMSO-d₆/D₂O): δ 10.66(s, 1H), 9.19(bs, 2H), 8.86(bs, 2H), 8.69(t, J= 5.5Hz, 1H), 8.13(d, J= 2Hz, 1H), 8.02(dd, J= 8 and 2Hz, 1H), 7.72(m, 4H), 7.38(m, 6H), 7.17(d, J= 2.6Hz, 1H), 7.03(d, J= 8.5Hz, 1H), 6.87(dd, J= 8.5 and 2.5Hz, 1H), 5.39(t, J= 4.7Hz, 1H), 5.08(s, 2H), 4.30 (m, 2H), 3.13(t, J= 6.5Hz, 2H), 1.87(m, 1H), 0.91(d, J= 6.5Hz, 6H); MS (ES⁺) 551.4 208

—H 205 S-2 ¹HNMR (DMSO-d₆): δ 11.26(s, 0.6H), 11.20(bs, 0.4H), 9.15(bs, 1.2H), 9.11(bs, 0.8H), 8.84(bs, 1.2H), 8.82(bs, 0.8H), 8.67(t, J= 5.6Hz, 0.6H), 8.58(t, J= 5.6Hz, 0.4H), 8.3(s, 1H), 8.12(d, J= 2Hz, 0.6H), 8.04(d, J= 2Hz, 0.4H), 7.96(dd, J= 2 and 8Hz, 1H), 7.84(m, 1H), 7.70(m, 2H), 7.57(m, 3H), 7.40(m, 4H), 7.22(m, 2H), 7.02(m, 2H), 5.21(s, 0.8H), 5.11(s, 1.2H), 3.12(t, J= 6.5Hz, 1.2H), 3.06(t, J= #6.5Hz, 0.8H), 1.84(m, 1H), 0.90(d, J= 6.5Hz, 3.6H), 0.86(d, J= 6.5Hz, 2.4H); MS (ES+): 564.5

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 217 —OCH₃

—Br 216 A-3 ¹H NMR(DMSO-d₆): δ 8.48(t, J=6.2Hz, 1H), 8.06(d, J=8.3Hz, 1H), 7.69(d, J=8.5Hz, 1H), 4.01(s, 3H), 3.15(t, J=6.5Hz, 2H), 1.91(m, 1H), 0.91(d, J=6.6Hz, 6H); MS(ES⁺): 287.1 218 —OCH₃

—CH═CH₂ 217 D-12 ¹H NMR(CDCl₃): δ 8.08(m, 2H), 7.20(m, 2H), 6.39(dd, J=2.0 and 17.3Hz, 1H), 5.53(dd, J=2.0 and 10.9Hz, 1H), 4.01(s, 3H), 3.15(t, J=6.5Hz, 2H), 1.91(m, 1H), 0.91(d, J=6.6Hz, 6H) 219 —OH

—CO₂CH₃ 218 E-2, V- 3, W-2 ¹H NMR(DMSO-d₆): δ 11.05(s, 1H), 8.48(t, J=6.2Hz, 1H), 8.06(d, J=8.7Hz, 1H), 7.53(d, J=8.5Hz, 1H), 3.90(s, 3H), 3.12(t, J=6.6Hz, 2H), 1.85(m, 1H), 0.86(d, J=6.6Hz, 6H); MS(ES⁺): 253.2 220 —OSO₂CF₃

—CO₂CH₃ 219 B-2 MS(ES⁺): 407.2 (M + Na)⁺ 237

—NH₂ —H 236 AF-1 MS(ES⁺): 137.1

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 221 —CHO —OBn —CH₃ 220 + 6 D-2 ¹H NMR(CDCl₃): δ 9.77(s, 1H), 8.40(d, J=7.9Hz, 1H), 8.13(d, J=6.8Hz, 1H), 7.83(d, J=7.9Hz, 1H), 7.61(d, J=2.60Hz, 1H), 7.20(m, 5H), 7.21(m, 1H), 7.18(d, J=8.3Hz, 1H), 5.18(s, 2H), 3.72(s, 3H), 3.35(q, J=5.8Hz, 2H), 1.96(m, 1H), 1.01(d, J=6.8Hz, 6H); MS(ES⁺): 447.4 222 —CO₂H —OBn —CH₃ 221 E MS(ES⁻): 461.3 223 —CO₂MEM —OBn —CH₃ 222 F MS(ES⁺): 573.33 (M + Na)⁺ 224 —CO₂MEM —OH —CH₃ 223 G MS(ES⁺): 461.36 225 —CO₂MEM —OSO₂CF₃ —CH₃ 224 B-2 MS(ES⁺): 615.58 (M + Na)⁺ 226 —CO₂MEM —CH═CH₂ —CH₃ 225 D-3 or D-12 MS(ES⁻): 381.35 [(M − MEM) − 1] 227 —CO₂H —CH═CH₂ —CH₃ 226 I-1 MS(ES⁻): 381.35 228

—CH═CH₂ —CH₃ 227 J MS(ES⁺): 500.35 229

—CH═CH₂ —H 228 I-2 MS(ES⁺): 486.32 245 —CHO —OH —CH₃ 221 AD MS(ES⁺): 357.40 246 —CHO —OSO₂CF₃ —CH₃ 245 B-2 Characterized in the next step 247 —CHO —CH═CH₂ —CH₃ 246 D-3 MS(ES⁺): 367.42 248

—CH═CH₂ —H 247 AE-3 MS(ES⁺): 472.39 249

—OBn —CH₃ 222 J MS(ES⁺): 580.4 250

—OBn —H 249 I-2 MS(ES⁺): 566.4 MS(ES⁻): 564.3 251

—OH —H 250 G MS(ES⁺): 476.3 MS(ES⁻): 474.2 252

—CH═CH₂ —H 247 AE-3 MS(ES⁺): 473.44 MS(ES⁻): 471.43

Cpd. Starting Method No. —R From Used Analytical Data 231b —CO₂CH₃ 230 AG-3 ¹H NMR(CDCl₃): δ 10.17(d, J=0.75Hz, 1H), 7.62(d, J=8.3Hz, 1H), 6.94(dd, J=8.3, 0.75Hz, 1H), 6.51(s, 1H), 3.90(s, 3H)

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 232a —H —CHO —CH₃ 231a + 6a D-6 or D-7 ¹H NMR(CDCl₃): δ 9.64(s, 1H), 8.44(d, J=2Hz, 1H), 8.02(dd, J=8 and 2Hz, 1H), 7.60(d, J=8.3Hz, 1H), 7.40(d, J=8Hz, 1H), 6.96(d, J=8Hz, 1H), 6.32(t, J=6 and 5Hz, 1H), 6.01(s, 2H), 3.72(s, 3H), 3.33(t, J=6.5Hz, 2H), 1.93(m, 1H), 1.00(d, J=6.8Hz, 6H); MS(ES⁺): 384.3 and 406.3 (M + Na)⁺ 232b —CO₂H —CHO —CH₃ 231b + 6a D-6 or D-7 ¹H NMR(DMSO-d₆): δ 9.87(s, 1H), 9.49(s, 1H), 8.64(d, J=2Hz, 1H), 8.3(s, 1H), 7.97(d, J=8Hz, 1H), 7.43(dd, J=8 and 2.6Hz, 1H), 7.35(m, 2H), 6.94(m, 1H), 6.05(s, 0.4H), 5.98(s, 0.6H), 3.55(s, 1.8H), 3.52(s, 1.2H), 3.02(t, J=6.5Hz, 2H), 1.78(m, 1H), 0.81(d, J=6.6Hz, 6H); MS(ES⁻): 426.2 233a —H —CO₂H —CH₃ 232a E ¹H NMR(DMSO-d₆): δ 12.29(bs, 1H), 8.69(t, J=5.5Hz, 1H), 8.38(d, J=2Hz, 1H), 8.03(dd, J=8 and 2Hz, 1H), 7.58(d, J=8.5Hz, 1H), 7.36(d, J=8Hz, 1H), 7.00(d, J=8.5Hz, 1H), 6.02(s, 2H), 3.64(s, 3H), 3.12(t, J=6.5Hz, 2H), 1.87(m, 1H), 0.91(d, J=6.8Hz, 6H); MS(ES⁻): 398.2 233b —CO₂H —CO₂H —CH₃ 232b E ¹H NMR(DMSO-d₆): δ 8.64(t, J=5.5Hz, 1H), 8.38(d, J=4Hz, 1H), 8.00(dd, J=8.5 and 4Hz, 1H), 7.59(dd, J=8.5 and 4Hz, 1H), 7.30(dd, J=8 and 2.5Hz, 1H), 6.52(s, 0.5H), 6.48(s, 0.5H), 3.60(s, 1.5H), 3.58(s, 1.5H), 3.08(t, J=6.5Hz, 2H), 1.84(m, 1H), 0.88(d, J=6.8Hz, 6H) 234a —H

—CH₃ 233a J MS(ES⁺): 517.4 234b —CO₂H

—CH₃ 233b J ¹H NMR(DMSO-d₆): δ 12.41(bs, 1H), 11.09(s, 1H), 10.96(s, 1H), 9.22(bs. 2H), 8.96(bs, 2H), 8.70(m, 1H), 8.38(dd, J=2 and 13Hz, 1H), 8.04(d, J=8Hz, 1H), 7.82(m, 4H), 7.65(dd, J=8 and 5Hz, 1H), 7.39(dd, J=8 and 2.5Hz, 1H), 7.11(dd, J=8.5 and 1.7Hz, 1H), 6.05(s, 1H), 3.67(s, 1.5H), 3.50(s, 1.5H), 3.10(t, J=6.5Hz, # 2H), 1.88(m, 1H), 0.90(d, J=6.8Hz, 6H) 235a —H

—H 234a I-2 ¹H NMR(DMSO-d₆ + DCl one drop): δ 8.34(d, J=2Hz, 1H), 7.97(dd, J=8 and 2Hz, 1H), 7.75(m, 4H), 7.33(dd, J=3.8 and 8.1Hz, 2H), 7.04(d, J=8.1Hz, 1H), 6.01(d, J=6Hz, 2H), 3.07(t, J=6.5Hz, 2H), 1.83(m, 1H), 0.86(d, J=6.8Hz, 6H); MS(ES⁻) 501.3; (ES+) 503.3

Cpd. Starting Method No. —R —R′ —R″ From Used Analytical Data 240 —CH(OH)—CH₂OH —Boc —CH₃ 161d L ¹H NMR(DMSO-d6): δ 10.47(s, 1H), 9.07(s, 2H), 8.72(t, J=5.7Hz, 1H), 8.29(d, J=2Hz, 1H), 8.08(dd, J=8.0, 2Hz, 1H), 7.95(s, 1H), 7.92(s, 1H), 7.67(m, 2H), 7.62(d, J=6.5Hz, 1H), 7.46(d, J=8Hz, 1H), 7.31(d, J=8Hz, 1H), 5.50(d, J=4.5Hz, 1H), 4.91(t, J=5.7Hz, 1H), 4.74(m, 1H), 4.25(s, 1H), 3.63(s, 3H), 3.15(t, J=6.4Hz, 2H), 1.91(m, 1H), 1.50(s, 9H), 0.95(d, J=6.7Hz, 6H) 241 —CHO —Boc —CH₃ 240 M ¹H NMR(DMSO-d6): δ 10.69(s, 1H), 10.17(s, 1H), 9.10(bs, 2H), 8.72(t, J=5.7Hz, 1H), 8.30(d, J=1.5Hz, 1H), 8.22(d, J=1.5Hz, 1H), 8.22(dd, J=1.5 and 8Hz, 1H), 8.07(dd, J=1.5 and 8Hz, 1H), 7.89(s, 1H), 7.86(s, 1H), 7.65(s, 1H), 7.62(s, 1H), 7.57(d, J=8Hz, 1H), 7.44(d, J=8Hz, 1H), 3.57(s, 3H), 3.11(t, J=6.4Hz, 2H), 1.85(m, 1H), 1.44(s, 9H), 0.89(d, J=6.7Hz, 6H) 242 —CH(OH)—CH═CH₂ —Boc —CH₃ 241 AG MS(ES⁺): 629.39 243 —CH(OH)—CH═CH₂ —H —CH₃ 242 S MS(ES⁺): 529.38 244 —CH(OH)—CH═CH₂ —H —H 243 I-2 MS(ES⁻): 515.35

Cpd. Starting Method No. —R From Used Analytical Data 254

253 AE-3 MS(ES⁺): 318.2, 320.2 255

254 R MS(ES⁺): 418

Cpd. Starting Method No. X —R From Used Analytical Data 258a H

131 AE-3 ¹H NMR(DMSO-d₆): δ11.71(bs, 1H), 8.57(t, J=5.5Hz, 1H), 8.44(s, 1H), 8.34(s, 1H), 7.80(dd, J=1.5, 7.5Hz, 1H), 7.45(d, J=12.8Hz, 1H), 7.20(m, 5H), 6.96(m, 1H), 4.13(m, 2H), 3.09(t, J=6.8Hz, 2H), 1.87(m 1H), 0.87(d, J=6.8Hz, 6H); MS(ES⁺) 463.62. 258b —CH═CH₂

187a AE-3 ¹H NMR (DMSO-d₆): δ10.01(s, 1H), 8.73(s, 2H), 8.39(d, J=2Hz, 1H), 8.33(s, 1H), 8.07(dd, J=7.7 & 2Hz, 1H), 7.78(m, 2H), 7.60(m, 2H), 7.40(m, 2H), 7.05(m, 2H), 6.7(dd, J=11 & 17.5, 1H), 6.34(t, J=6Hz, 1H), 6.26(d, J=8Hz, 1H), 5.73(d, J= 17.5Hz, 1H), 5.24(d, J=11Hz, 1H), 4.11(t, J=5.5Hz, 2H), # 3.11(t, J=6Hz, 2H), 1.87(m, 1H), 0.90(t, J=6.6Hz, 6H); MS(ES⁺) 487.35. 258c —CH═CH₂

187a AE-3 ¹H NMR(DMSO-d₆): δ8.78(s, 2H), 8.73(t, J=5.5Hz, 1H), 8.40(d, J=2Hz, 1H), 8.37(s, 2H), 8.08(s, 1H), 7.48-7.32(m, 5H), 7.28(d, J=7.5Hz, 1H), 6.68(m, 1H), 6.55(t, J=5.5Hz, 1H), 6.30(d, J=8.6Hz, 1H), 6.01(m, 1H), 5.71(d, J=17.5Hz, 1H), 5.23(d, J= 11Hz, 1H), 5.11(m, 2H), 4.13(d, J=5.3Hz, 2H), 3.11(t, # J=6.5Hz, 2H), 1.87(m, 1H), 0.91(d, J=6.8Hz, 6H); MS(ES⁺) 511.41 258d —CH═CH₂

187a AE-3 ¹H NMR(DMSO-d₆): δ8.62(t, J=5.7Hz, 2H), 8.52(s, 2H), 8.31(s, 1H), 7.88(s, 1H), 7.68(s, 1H), 7.24(m, 5H), 7.00(d, J=6.1Hz, 1H), 6.72(q, J=11.2Hz, 1H), 6.48(s, 1H), 5.73(d, J=16.8Hz, 1H), 5.22(d, J=10.5Hz, 1H), 4.08(m, 2H), 3.10(t, J=6.1Hz, 2H), 1.86(m, 1H), 0.89(d, J=6.8Hz, 6H); MS(ES+) 489.39. 258e —CH═CH₂

187a AE-3 ¹H NMR(DMSO-d₆): δ8.61(t, J=5.3Hz, 4H), 8.32(s, 1H), 8.18(s, 1H), 7.89(t, J=8.5Hz, 2H), 7.70(s, 1H), 7.32(d, J=8.1Hz, 1H), 7.25(m, 3H), 6.97(d, J=7.5Hz, 1H), 6.68(q, J=17.8 & 10.9Hz, 1H), 5.67(d, J=17.6Hz, 1H), 5.18(d, J=10.9Hz, 1H), 4.24(m, 2H), 3.10(t, J=6.5Hz, 2H), 1.88(m, 1H), 0.90(d, J=6.8Hz, 6H); MS(ES+) 472.37. 258f —CH═CH₂

187a AE-3 ¹H NMR(DMSO-d₆): δ8.60(s, 1H), 8.38(s, 2H), 7.81(s, 1H), 7.30(d, J=7.7Hz, 2H), 7.17(m, 4H), 7.13(d, J=5.7Hz, 1H), 7.05(m, 1H), 6.69(m, 2H), 5.64(d, J=16.6Hz, 1H), 5.16(d, J=11.2Hz, 1H), 4.27(m, 1H), 3.91(m, 4H), 3.10(t, J=6.5Hz, 2H), 1.86(m, 1H), 0.90(d, J=6.6Hz, 6H); MS(ES⁺) 501.37. 258g —CH═CH₂

187a AE-3 ¹H NMR(DMSO-d₆): δ13.84(br s, 2H), 9.32(s, 2H), 9.11(s, 2H), 8.56(t, J=6.4Hz, 1H), 7.81-7.41(m, 8H), 7.11(d, J=7.9Hz, 1H), 6.86(dd, J=11.1 and 17.3Hz, 1H), 5.97(d, J=17.3Hz, 1H), 5.38(d, J=11.1Hz, 1H), 3.12(m, 2H), 1.87(m, 1H), 0.87(d, J=6.4Hz, 6H); MS(ES⁺): 520.5.

Cpd. Starting Method No. R R′ Y From Used Analytical Data 259 CH₃ CH₃ CN 74 AM MS(ES⁺): 522.3(M + Na) 260 H H

259 AJ-1, I-2 ¹H NMR(DMSO-d₆): δ8.76(bs, 2H), 8.40(bs, 2H), 8.35(m, 1H), 8.08(d, J=7Hz, 1H), 7.87(m, 1H), 7.79(d, J=6Hz, 1H), 7.42-7.64(m, 5H), 7.30(m, 1H), 7.16(m, 1H), 7.05(m, 1H), 6.70(t, J=3.5Hz, 1H), 6.45(m, 1H), 3.86(s, 1.5H), 3.75(s, 1.5H), 3.10(t, J=6.7Hz, 2H), 1.88(m, 1H), 0.90(d, J=6.7Hz, 6H); MS(ES⁺) 519.35

It was prepared as shown in Schemes 31 and 31a. Analytical: ¹H NMR (DMSO-d₆): δ 13.05 (br s, 1H), 9.09 (s, 2H), 8.94 (s, 2H), 8.65 (m, 1H), 8.26-7.60 (m, 8H), 7.20 (m, 1H), 6.90 (dd, J=11.1 and 17.3 Hz, 1H), 6.00 (d, J=17.3 Hz, 1H), 5.40 (d, J=11.1 Hz, 1H), 3.25 (m, 2H), 1.59 (q, J=6.9 Hz, 2H), 0.92 (t, J=7.3 Hz, 3H); MS (ES⁻): 470.30.

Cpd. Starting Method No. X Y R From Used Analytical Data 263a H CHO CH₃ 261 and D-1 MS(ES⁺): 241.2 262a 263b

CHO CH₃ 261 and 3a D-1 MS(ES⁺): 340.3 264a H CO₂H CH₃ 263a E MS(ES⁻): 255.5 264b

CO₂H CH₃ 263b E MS(ES⁺): 356.3 265a H

H 264a J, I-2 ¹H NMR (DMSO-d₆), MSA salt): δ10.39(s, 1H), 8.6(s, 2H), 8.45(s, 2H), 7.12-7.65(m, 4H), 7.66-8.2(m, 8H), 2.35(s, 3H); MS(ES⁺) 360.33. 265b

H 264b J, I-2 ¹H NMR(DMSO-d₆): δ13.01(bs, 1H), 10.74(s, 1H), 9.22(s, 2H), 8.88(s, 2H), 8.61(t, J=5.5Hz, 1H), 8.1(dd, J=8.2 and 2Hz, 1H), 8.02(m, 3H), 7.86(m, 1H), 7.83(s, 1H), 7.61(m, 3H), 3.19(t, J=6.7Hz, 2H), 2.32(s, 3H), 1.82(m, 1H), 0.92(d, J=6.59Hz, 6H); MS(ES⁺) 459.29. 266a H

H 263a AE-3 ¹H NMR(DMSO-d₆ MSA salt): δ8.75(s, 2H), 8.40(s, 2H), 7.15-7.75(m, 12H), 4.40(s, 2H), 2.5(s, 3H); MS(ES⁺) 346.37. 266b

H 263b AE-3 ¹H NMR(DMSO-d₆): δ8.77(s, 2H), 8.39(s, 2H), 8.22(s, 1H), 7.6-7.2(m, 10H), 6.7(d, J=4.8Hz, 2H), 4.4(b, 2H), 2.99(m, 2H), 2.49(s, 3H), 1.88(m, 1H), 0.88(d, J=6.58Hz, 6H); MS(ES⁺) 445.32.

The following non-limiting examples are presented to further illustrate the present invention.

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-thien-2-yl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-thien-3-yl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-1,1′:4′,1″-terphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(3-furyl)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-pyridin-4-yl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-(1H-pyrrol-2-yl)-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-[2-(hydroxymethyl)thien-3-yl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-[3-(hydroxymethyl)thien-2-yl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

4′-Allyl-2′-[({4-[amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylate

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-(1,3-thiazol-2-yl)-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-[3-(hydroxymethyl)-2-furyl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-prop-1-ynyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(3-hydroxy-3-methylbut-1-ynyl)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(3-methylbutanoyl)amino]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(4-hydroxybut-1-ynyl)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-[(1E)-3-methylbuta-1,3-dienyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(3-hydroxyprop-1-ynyl)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(2-furyl)-4-[(propylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(sec-butylamino)carbonyl]-4′-(2-furyl)-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(2-furyl)-4-{[(2,2,2-trifluoroethyl)amino]carbonyl}-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-(2-furyl)-4-{[(4-hydroxybutyl)amino]carbonyl}-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(ethylamino)carbonyl]-4′-(2-furyl)-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-5′-methoxy-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-(thien-2-ylmethyl)-1,1′-biphenyl-2-carboxylic acid

2-{3-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]pyridin-4-yl}-5-[(isobutylamino)carbonyl]benzoic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(cyclopentylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-5′-ethoxy-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

Methyl 2′-[({4-[({[(acetyloxy)methoxy]carbonyl}amino)(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylate

Methyl 2′-[({4-[{[(benzyloxy)carbonyl]amino}(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylate

N¹-{4-[Amino(imino)methyl]phenyl}-N8-isobutyl-6-oxo-6H-benzo[c]chromene-1,8-dicarboxamide

2′-[({4-[Amino(imino)methyl]phenyl}amino)methyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-({[4-(4,5-Dihydro-1H-imidazol-2-yl)phenyl]amino}carbonyl)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-5′-thien-2-yl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-5′-(2-amino-2-oxoethoxy)-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4′-ethoxy-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

2-{5-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-1,3-benzodioxol-4-yl}-5-[(isobutylamino)carbonyl]benzoic acid

2′-[-({4-[Amino(imino)methyl]phenyl}amino)ethyl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

3-[2-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-(benzyloxy)phenyl]-6-[(isobutylamino)carbonyl]pyridine-2-carboxylic acid

3-[2-(4-Carbamimidoyl-phenylcarbomoyl)-4-vinyl-phenyl]-6-isobutylcarbamoyl-pyridine-2-carboxylic acid

2′-[(5-Carbamimidoyl-pyridin-2-ylamino)-methyl]-4-isobutylcarbamoyl-4′-vinyl-biphenyl-2-carboxylic acid

2′-{[4-N-Hydroxycarbamimidoyl)-phenylamino]-methyl}-4-isobutycarbamoyl-4′-vinyl-biphenyl-2-carboxylic acid

2′-{[4-(N-Hydroxycarbamimidoyl)-phenylamino]-methyl}-4-isobutylcarbamoyl-4′-vinyl-biphenyl-2-carboxylic acid methyl ester

3-{2-[(4-Carbamimidoyl-phenylamino)-methyl]-4-vinyl-phenyl}-6-isobutylcarbamoyl-pyridine-2-carboxylic acid

Methyl 3-{2-[({4-[(hydroxyamino)(imino)methyl]phenyl}amino)methyl]-4-vinylphenyl}-6-[(isobutylamino)carbonyl]pyridine-2-carboxylate

Methyl 3-{2-[({4-[(hydroxyamino)(imino)methyl]phenyl}amino)carbonyl]-4-vinylphenyl}-6-[(isobutylamino)carbonyl]pyridine-2-carboxylate

N²-Hydroxy-3-{2-[({4-[(hydroxyamino)(imino)methyl]phenyl}amino)carbonyl]-4-vinylphenyl}-N6-isobutylpyridine-2,6-dicarboxamide

3-{2-[({4-[(Hydroxyamino)(imino)methyl]phenyl}amino)carbonyl]-4-vinylphenyl}-6-[(isobutylamino)carbonyl]pyridine-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)methyl]-4-[(isobutylamino)carbonyl]-5′-methoxy-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)(carboxy)methyl]-4-[(isobutylamino)carbonyl]-5′-methoxy-1,1′-biphenyl-2-carboxylic acid

2′-[({5-[(Hydroxyamino)(imino)methyl]pyridin-2-yl}amino)methyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-{[(3-carboxypropyl)amino]carbonyl}-4′-(2-furyl)-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-{[(3-carboxypropyl)amino]carbonyl}-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

3-{2-[({4-[Amino(imino)methyl]phenyl}amino)methyl]-5-methoxy-4-vinylphenyl}-6-[(isobutylamino)carbonyl]pyridine-2-carboxylic acid

3-{2-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-5-methoxy-4-vinylphenyl}-6-[(isobutylamino)carbonyl]pyridine-2-carboxylic acid

2′-(4-Carbamimidoyl-phenylcarbamoyl)-4-(2-carboxy-ethylcarbamoyl)-4′-ethylbiphenyl-2-carboxylic acid

2′-[({5-[Amino(imino)methyl]pyridin-2-yl}amino)methyl]-4-[(isobutylamino)carbonyl]-5′-methoxy-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({6-[Amino(imino)methyl]pyridin-3-yl}amino)methyl]-4-[(isobutylamino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

3′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

3′-[({4-[Amino(imino)methyl]phenyl}amino)methyl]-4-[(isobutylamino)carbonyl]-1,1′-biphenyl-2-carboxylic acid

4-{[(2-Aminoethyl)amino]carbonyl}-2′-[({4-[amino(imino)methyl]phenyl}amino)carbonyl]-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-[({4-[Amino(imino)methyl]phenyl}amino)carbonyl]-4-{[(2,3-dihydroxypropyl)amino]carbonyl}-4′-vinyl-1,1′-biphenyl-2-carboxylic acid

2′-(4-Carbamimidoyl-phenylcarbamoyl)-4-(2-carbamoyl-ethylcarbamoyl)-4′-ethylbiphenyl-2-carboxylic acid

Biological Assay Methods

In Vitro Assay for Inhibition of TF/FVIIa

To assess the inhibition of the test compounds against the target enzyme, TF/FVIIa, an amidolytic assay based upon the absorbance of p-Nitroanalide (pNA) at OD₄₀₅ was utilized. The IC₅₀ of the test compounds was determined by using KC4A data reduction software (Bio-Tek Instruments) to interpolate percent inhibition from observed Vmax values.

TF/FVIIa assay reactions were performed in a 200 μL mixture containing 4 nM FVIIa, 10 nM lipidated tissue factor, in an assay buffer containing 100 mM Tris, pH 7.2, 150 mM NaCl, 5 mM calcium chloride, 0.1% bovine serum albumin (BSA), and 10% dimethyl sulfoxide (DMSO). TF and FVIIa were allowed to equilibrate at room temperature for 15 minutes. Test compounds dissolved in DMSO were incubated at varied concentrations with TF/FVIIa for 10 minutes, followed by addition of 500 □M substrate Spectrozyme-FVIIa. Reactions were incubated for 5 minutes at room temperature prior to measuring the change in OD₄₀₅ nm for 10 minutes at 21 second intervals with a Powerwave _(x) (Bio-Tek Instruments) microplate reader.

In Vitro Assay for Human Thrombin

This colorimetric assay was used to assess the ability of the test compounds to inhibit the human thrombin enzyme. IC₅₀ of the test compounds was determined by using KC4A data reduction software (Bio-Tek Instruments) to interpolate percent inhibition from observed Vmax values.

Thrombin assay reactions were performed in a 200 μL mixture containing human thrombin at (1 U/mL) in an assay buffer containing 100 mM HEPES, 10 mM calcium chloride, and 10% DMSO, pH 7.5. Test compounds dissolved in DMSO were added to thrombin enzyme reactions at varied concentrations, followed by the addition of substrate Nα-Benzoyl-Phe-Val-Arg-p-Nitroanilide at a final concentration of 1 mM. Reactions were incubated for 5 minutes at room temperature prior to measuring the change in OD₄₀₅ nm for 10 minutes at 21 second intervals with a Powerwave _(x) (Bio-Tek Instruments) microplate reader.

In Vitro Assay for Human Trypsin

This enzymatic assay was employed to evaluate the ability of the test compounds to inhibit human pancreatic trypsin. IC₅₀ of the test compounds was determined by using KC4A data reduction software (Bio-Tek Instruments) to interpolate percent inhibition from observed Vmax values.

Trypsin assay reactions were performed in a 200 μL mixture containing human pancreatic trypsin at 1 μg/mL in an assay buffer containing 200 mM triethanolamine (TEA), 10 mM calcium chloride, 10% DMSO, pH 7.8. Test compounds dissolved in DMSO were added to trypsin enzyme reactions at varied concentrations, followed by the addition of substrate Nα-Benzoyl-L-Arginine p-Nitroanilide (L-BAPNA) at a final concentration of (0.25 mg/mL). Reactions were incubated for 5 minutes at room temperature prior to measuring the change in OD₄₀₅ nm for 10 minutes at 21 second intervals with a Powerwave _(x) (Bio-Tek Instruments) microplate reader.

Biological Data

IC₅₀ Values of Some Selected Compounds on Different Serine Protease Enzymes

R (With Respect to Phenyl Ring R′ TF/FVIIa Trypsin Thrombin

++ + +

++ + +

++ + +

++ − −

+ − −

++ − −

+++ ++ +

+++ ++ +

+++ ++ +

+++ ++ +

IC₅₀ values: +means>1 μM; ++means>100 nM; +++means<100 nM

A comparison of Examples with R group and without R group illustrates the greatly-enhanced activity achieved pursuant to the present invention.

Compounds of the present invention are useful as inhibitors of trypsin-like serine protease enzymes such as thrombin, factor VIIa, TF/FVIIa, and trypsin.

These compounds may be employed to inhibit the coagulation cascade and prevent or limit coagulation.

These compounds may be used to inhibit the formation of emboli or thromboli in blood vessels.

These compounds may be used to treat thrombolymphangitis, thrombosinusitis, thromboendocarditis, thromboangitis, and thromboarteritis.

These compounds may be used to inhibit thrombus formation following angioplasty. These may be used in combination with other antithrombolytic agents such as tissue plasminogen activators and their derivatives, streptokinase and its derivatives, or urokinase and its derivatives to prevent arterial occlusion following thrombolytic therapy.

These compounds may also be used in metastatic diseases, or for any disease where inhibition of coagulation is indicated.

These compounds may be used as diagnostic reagents in vitro for inhibiting clotting of blood in the tubes.

These compounds may be used alone or in combination with other compounds such as heparin, aspirin, or warfarin and any other anticoagulant agents.

These compounds may be used as anti-inflammatory agents.

According to a further aspect of the invention, compounds may be employed in preventing ex vivo coagulation such as that encountered in the extracorporeal perfusion of blood through for example artificial valves, prothesis, stents or catheters. According to this aspect of the invention the extracorporeal device may be coated with the compositions of the invention resulting in a lower risk of clot formation due to extrinsic pathway activation.

Dosage and Formulation

The compounds of this invention can be administered by any means that produces contact of the active agent's site of action with factor VIIa and other serine proteases in the body of a human, mammal, bird, or other animal. They can be administered by any conventional means, such as oral, topical, transdermal, parenteral, subcutaneous, intraperitoneal, intrapulmonary, and intranasal, available for use in conjunction with pharmaceuticals, either as individual therapeutic agents or in a combination of therapeutic agents. Parenteral infusion includes intramuscular, intravenous, and intraarterial. They can be administered alone, but generally administered with a pharmaceutical carrier elected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage administered will, or course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the age, health and weight of the recipient; the nature and extent of the symptoms, the kind of concurrent treatment; the frequency of treatment; and the effect desired. A daily dosage of active ingredient can be expected to be about 0.0001 to 1000 milligram (mg) per kilogram (kg) of body weight, with the preferred dose being 0.1 to about 30 mg/kg.

Dosage forms (compositions suitable for administration) contain from about mg to about 500 mg of compound per unit. In these pharmaceutical compositions, the compound of the present invention will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.

The daily dose of the compounds of the invention that is to be administered can be a single daily dose or can be divided into several, for example, two, three or four, part administrations. The pharmaceutical compositions or medicaments of the invention can be administered orally, for example in the form of pills, tablets, lacquered tablets, coated tablets, granules, hard and soft gelatin capsules, solutions, syrups, emulsions, suspensions or aerosol mixtures. Administration, however, can also be carried out rectally, for example in the form of suppositories, or parenterally, for example intravenously, intramuscularly or subcutaneously, in the form of injection solutions or infusion solutions, microcapsules, implants or rods, or percutaneously or topically, for example in the form of ointments, solutions or tinctures, or in other ways, for example in the form of aerosols or nasal sprays.

Gelatin capsules contain a compound of the present invention and powdered carriers, such as lactose, starch, cellulose derivatives, biocompatible polymers, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated to mask by unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.

Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance. They may also contain buffering agents, surfactants and preservatives. Liquid oral products can be developed to have sustained-release properties. They may also contain cyclodextrin derivatives to enhance the solubility of the active ingredient and to promote its oral uptake.

In general, water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water-soluble salt of the active ingredient, suitable stabilizing agents, and, if necessary, buffering agents. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents. Also used are citric acid and its salts and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propylparaben, and chlorobutanol.

Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing Company and in the Handbook of Pharmaceuticals Excipients, American Pharmaceutical Association, both standard reference texts in this field.

Useful pharmaceutical dosage forms for administration of the compounds according to the present invention can be illustrated as follows:

Hard Shell Capsules

A large number of unit capsules are prepared by filling standard two-piece hard gelatin capsules each with 100 mg of powdered 1500 mg of lactose, 50 mg of cellulose, and 6 mg of magnesium stearate.

Soft Gelatin Capsules

A mixture of active ingredient in a digestible oil such as soybean oil, cottonseed oil, or olive oil is prepared and injected by means of a positive displacement pump into molten gelatin to form soft gelatin capsules containing 100 mg of the active ingredient. The capsules are washed and dried. The prodrug can be dissolved in a mixture of polyethylene glycol, glycerin and sorbitol to prepare a water miscible medicine mix.

Tablets

A large number of tablets are prepared by conventional procedures so that the dosage unit was 100 mg of active ingredient, 0.2 mg of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of microcystalline cellulose, 11 mg of starch, and 9.98 mg of lactose. Appropriate aqueous and non-aqueous coatings may be applied to increase palatability improve elegance and stability or delay absorption.

Immediate Release Tablets/Capsules

These are solid oral dosage forms made by conventional and novel processes. These units are taken orally without water for immediate dissolution and delivery of the medication. The drug is mixed containing ingredient such as sugar, gelatin, pectin, and sweeteners. These liquids are solidified into solid tablets or caplets by freeze drying and solid thermoelastic sugars and polymers or effervescent components to produce porous matrices intended for immediate release, without the need of water.

Moreover, the compounds of the present invention can be administered in the form of nose drops, metered dose nasal or buccal inhalers. The drug is delivered from a nasal solution as a fine mist or from a powder as an aerosol.

In another embodiment of the invention, a compound of the invention can be used in an assay to identify the presence of factor VIIa and other serine protease or to isolate factor VIIa and other serine protease in a substantially purified form. For example, the compound of the invention can be labeled with, for example, a radioisotope, and the labeled compound is detected using a routine method useful for detecting the particular label. In addition, a compound the invention can be used advantageously as a probe to detect the location or amount of factor VIIa and other serine protease activity in vivo, in vitro or ex vivo.

Various modifications of the invention in addition to those shown and described herein will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims.

The foregoing disclosure includes all the information deemed essential to enable those skilled in the art to practice the claimed invention. The foregoing description of the invention illustrates and describes the present invention. Additionally, the disclosure shows and describes only the preferred embodiments of the invention but, as mentioned above, it is to be understood that the invention is capable of use in various other combinations, modifications, and environments and is capable of changes or modifications within the scope of the inventive concept as expressed herein, commensurate with the above teachings and/or the skill or knowledge of the relevant art. The embodiments described hereinabove are further intended to explain best modes known of practicing the invention and to enable others skilled in the art to utilize the invention in such, or other, embodiments and with the various modifications required by the particular applications or uses of the invention. Accordingly, the description is not intended to limit the invention to the form disclosed herein. Also, it is intended that the appended claims be construed to include alternative embodiments. 

What is claimed is:
 1. Compound having the structure (I) shown below:

Each E¹ and L individually is a 5 to 7 membered saturated or unsaturated carbon ring, bicyclic saturated or unsaturated carbon ring, or 1-8 hydrocarbon chain which may be substituted with one or more hetero groups selected from N, O, S, S(O), and S(O₂) which may be saturated or unsaturated; R is —CH═CH—R²—, —C═C—R², —C(R²)═CH₂, —C(R²)═C(R³), —CH═NR², —C(R²)═N—R³, 4-7 membered saturated or unsaturated carbon ring system with or without substitution, 4-7 membered saturated or unsaturated hetero ring system with or without substitution, or chain of 2 to 8 carbon atoms having 1 to 5 double or triple bonds with substitutions selected from R¹, R² or R³; R¹ is H, —R, —NO₂, —CN, -halo, —N₃, —C₁₋₈ alkyl, —(CH₂)_(n)CO₂R², —C₂₋₈ alkenyl-CO₂R², —O(CH₂)_(n)CO₂R², —C(O)NR²R³, —P(O)(OR²)₂, alkyl substituted tetrazol-5-yl, —(CH₂)_(n)O(CH₂)_(n)aryl, —NR²R³, —(CH₂)_(n)OR², —(CH₂)_(n)SR², —N(R²)C(O)R³, —S(O₂)NR²R³, —N(R²)S(O₂)R³, —(CHR²)_(n)NR²R³, —C(O)R³, (CH₂)_(n)N(R³)C(O)R³, —N(R²)CR²R³ substituted or unsubstituted (CH₂)_(n)-cycloalkyl, substituted or unsubstituted (CH₂)_(n)-phenyl, or substituted or unsubstituted (CH₂)_(n)-heterocycle which may be saturated or unsaturated; m is 1 except that when E¹ is a cyclic ring of more than 5 atoms, then m is 1 or higher, depending upon the size of the ring; R² is H, -halo, -alkyl, -haloalkyl, —(CH₂)_(n)-phenyl, —(CH₂)₁₋₃-biphenyl, —(CH₂)₁₋₄—Ph—N(SO₂—C₁₋₂-alkyl)₂, —CO(CHR¹)_(n)—OR¹, —(CHR¹)_(n)-heterocycle, —(CHR¹)_(n)—NH—CO—R¹, —(CHR¹)_(n)—NH—SO₂R¹, —(CHR¹)_(n)—Ph—N(SO₂—C₁₋₂-alkyl)₂, —(CHR¹)_(n)—C(O)(CHR¹)—NHR¹, —(CHR¹)_(n)—C(S)(CHR¹)—NHR¹, —(CH₂)_(n)O(CH₂)_(n)CH₃, —CF₃, —C₂₋₅ acyl, —(CHR¹)_(n)OH, —(CHR¹)_(n)CO₂R¹, —(CHR¹)_(n)—O-alkyl, —(CHR¹)_(n)—O—(CH₂)_(n)—O-alkyl, —(CHR¹)_(n)—S-alkyl, —(CHR³)_(n)—S(O)-alkyl, —(CHR¹)_(n)—S(O₂)-alkyl, —(CHR¹)_(n)—S(O₂)—NHR³, —(CHR¹)_(n)—N₃, —(CHR³)_(n)NHR⁴, 2 to 8 carbon atom alkene chain having 1 to 5 double bonds, 2 to 8 carbon atom alkyne chain having 1 to 5 triple bonds, sustituted or unsubstituted-(CHR³)_(n) heterocycle, or substituted or unsubstituted-(CHR³)_(n) cycloalkyl which may be saturated or unsaturated; When n is more than 1, the substitutions R₁ and R³ may be same or different; R³ is H, —OH, —CN, substituted alkyl, —C₂₋₈ alkenyl, substituted or unsubstituted cycloalkyl, —N(R¹)R², or 5-6 membered saturated substituted or unsubstituted hetero ring; —NR²R³ may form a ring system having 4 to 7 atoms or may be bicyclic ring; wherein said ring system comprises carbon or hetero atoms and further it may saturated or unsaturated and also may be substituted or unsubstituted; W is a direct bond, —CHR²—, —CH═CR²—, —CR²═CH—, —CR²═CR²—, —C═C—, —O—CH²—, —CHR²—O—, —N(R²)—C(O)—, —C(O)—N(R²)—, —N(R²)—CH—(R³)—, —CH₂—N(R²)—, —CH(R¹)—N(R²)—, —S—CHR²—, —CHR²—S—, —S(O₂)—N(R²)—, —C(O)N(R²)—(CHR²)_(n)—, —C(R¹R²)_(n)—NR²—, —N(R²)—S(O₂)—, —R²C(O)NR², —R²NC(O)NR²—, —CONR²CO—, —C(═NR²)NR²—, —NR²C(═NR²)NR²—, —NR²O, —N═NCHR²—, or —C(O)NR²SO₂—; E² is 5 to 7 membered saturated or unsaturated carbon ring, 5 to 7 membered saturated or unsaturated hetero ring, bicyclic ring system, C₁₋₈ alkyl, C₂₋₈ alkenyl, C₂₋₈ alkynyl, alkylaryl, aralkyl, aralkenyl, aralkynyl, alkoxy, alkylthio, or alkylmino; each X individually is a direct bond, substituted or unsubstituted C₁₋₄ methylene chain, O, S, NR², S(O), S(O₂), or N(O) containing one or two C₁₋₄ substituted or unsubstituted methylene chains; X at different places may be same or different; B is H, -halo, —CN, —NH₂, —(CH₂)_(n)—C(—NR⁴)NHR⁵, —(CH₂)_(n)—NHR⁴, —(CH₂)_(n)NHC(═NR⁴)NR⁵, —(CH₂)_(n)—OR⁴, C₁₋₈ substituted or unsubstituted alkyl, substituted or unsubstituted ring system having 4 to 7 carbon or hetero atoms which may be saturated or unsaturated; B¹ is selected from B; B¹ and B may be same or different; There may be more than one similar or different R² groups present on E², when E² is a cyclic group of more than 5 atoms; p is 1 except that when E² is a cyclic ring of more than 5 atoms, p is 1 or higher depending upon the size of the ring; n is 0-4; A is selected from R¹; o is 1 except that when L is a cyclic ring of more than 5 atoms, o is 1 or higher depending upon the size of the ring; Each V and V¹ individually is selected from R₁ and N-alkyl substituted carboxamidyl (—CONHR) where the alkyl group may be straight, branched, cyclic, or bicyclic; N,N-disubstituted carboxamidyl of the formula —CONR₁R₂ where R₁ and R₂ may be substituted or unsubstituted alkyl or aryl and may be the same or different; mono- or disubstituted sulfonamides of the formula SO₂NHR or —SO₂NR₁R₂; and methylene- or polymethylene chain-extended variants thereof; Each R⁴ and R⁵ individually is H, —(CH₂)_(n)OH, —C(O)OR₆, —C(O)SR⁶, —(CH₂)_(n)C(O)NR⁷R⁸, —O—C(O)—O—R⁷, an amino acid or a dipeptide; Each R⁶ is H, R⁷, —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—R⁹, —(CH₂)_(n)—C(R⁷)(R⁸)—O—C(O)R⁹, —(CH₂)_(n)—C(R⁷)(R⁸)—O—C(O)—O—R⁹, or —C(R⁷)(R⁸)—(CH₂)_(n)—O—C(O)—O—R⁹; and Each R⁷, R⁸ and R⁹ individually is H, alkyl, substituted alkyl, aryl, substituted aryl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, heterocycle, substituted heterocycle, alkylaryl, substituted alkylaryl, cycloalkyl, substituted cycloalkyl, or CH₂CO₂alkyl.
 2. The compound of claim 1 presented by the structure:

Wherein R is selected from the group consisting of

R¹ is selected from the group consisting of H, OH, OCH₃, CHO, OSO₂CF₃, OCH₂—CH₂—OAc, O—CH₂CH₂—OH, OCH₂CO₂C₂H₅, OCH₂CO₂H, CO₂H, CH₂OH, OCH(CH₃)₂, OC(O)(CH₃)₃, OCH₂CONH₂,

R₂ is selected from the group consisting of CO₂-alkyl, CO₂-aryl, CO₂-arylalkyl, CO₂H, CH₂CO₂-alkyl, CH₂OH, CONH₂; R³ is selected from the group consisting of H, C(O)—NH—R₅, CO₂MEM, CO₂H,

R₄ is selected from the group consisting of C(O)NH—R₆, —CH(R₇)—NH—R₆, CO₂H, CHO, CO₂MEM, —CH(R₇)—O—R₆, —CH₂—CH₂—NH—R₆ R₅ is selected from the group consisting of

R₆ is selected from the group consisting of

R₇ is selected from the group consisting of H, CH₃, —(CH₂)_(n)—CO₂H, —(CH₂)_(n)—CO₂-alkyl wherein n=0-3; R₈ is selected from the group consisting of —CH₂—CCl₃, —CH₃, C₂H₅, CH₂C₆H₅, C(CH₃)₃,

and X is selected from CH, N; and pharmaceutically acceptable salts thereof; and prodrug thereof.
 3. The compound of claim 1 represented by the structure:

Wherein R is selected from the group consisting of

R₆ is selected from the group consisting of

R₁ is selected from the group consisting of H, OH, OCH₃, CHO, OSO₂CF₃, OCH₂—CH₂—OAc, O—CH₂—CH₂—OH, OCH₂CO₂C₂H₅, OCH₂CO₂H, CO₂H, CH₂OH, OCH(CH₃)₂, OC(O)(CH₃)₃, OCH₂CONH₂,

R₂ is selected from the group consisting of CO₂-alkyl, CO₂-aryl, CO₂-arylalkyl, CO₂H, CH₂CO₂-alkyl, CH₂OH, CONH₂; R₃ is selected from the group consisting of H, C(O)—NH—R₅, CO₂MEM, CO₂H,

R₄ is selected from the group consisting of C(O)NH—R₆, —CH(R₇)—NR₆, CO₂H, CHO, CO₂MEM, —CH(R₇)—O—R₆, —CH₂CH₂—NH—R₆ R₅ is selected from the group consisting of

R₇ is selected from the group consisting of H, CH₃, —(CH₂)_(n)—CO₂H, —(CH₂)_(n)—CO₂-alkyl wherein n=0-3; R₈ is selected from the group consisting of —CH₂—CCl₃, —CH₃, C₂H₅, CH₂C₆H₅, C(CH₃)₃,

and X is selected from CH, N; and pharmaceutically acceptable salts thereof; and prodrug thereof.
 4. The compound of claim 1 represented by the structure:

Wherein R is selected from the group consisting of

R₁ is selected from the group consisting of H, OH, OCH₃, CHO, OSO₂CF₃, OCH₂—CH₂—OAc, O—CH₂—CH₂—OH, OCH₂CO₂C₂H₅, OCH₂CO₂H, CO₂H, CH₂OH, OCH(CH₃)₂, OC(O)(CH₃)₃, OCH₂CONH₂,

R₂ is selected from the group consisting of CO₂-alkyl, CO₂-aryl, CO₂-arylalkyl, CO₂H, CH₂CO₂-alkyl, CH₂OH, CONH₂; R₃ is selected from the group consisting of H, C(O)—NH—R₅, CO₂MEM, CO₂H,

R₄ is selected from the group consisting of C(O)NH—R₆, —CH(R₇)—NH—R₆, CO₂H, CHO, CO₂MEM, —CH(R₇)—O—R₆, —CH₂—CH₂—NH—R₆ R₅ is selected from the group consisting of

R₆ is selected from the group consisting of

R₇ is selected from the group consisting of H, CH₃, —(CH₂)_(n)—CO₂H, —(CH₂)_(n)—CO₂-alkyl wherein n=0-3; R₈ is selected from the group consisting of —CH₂—CCl₃, —CH₃, C₂H₅, CH₂C₆H₅, C(CH₃)₃,

and X is selected from CH, N; and pharmaceutically acceptable salts thereof; and prodrug thereof.
 5. A pharmaceutical composition containing at least one compound according to claim
 1. 6. A method for inhibiting serine protease in a patient which comprises administering to the patient an effective serine protease inhibiting amount of at least one compound according to claim
 1. 7. A method for inhibiting the coagulation cascade and preventing or limiting coagulation by administering to a patient an effective amount of at least one compound according to claim
 1. 8. A method for inhibiting the formation of emboli or thromboli in blood vessels by administering to a patient an effective amount of at least one compound according to claim
 1. 9. A method for treating at least one condition selected from the group consisting of trombolymphangitis, thrombosinusitis, thromboendocarditis, thromboangitis, unstable angina, and thromboarteritis which comprises administering to a patient an effective amount of at least one compound according to claim
 1. 10. A method for inhibiting thrombus formation following angioplasty which comprises administering to a patient an effective amount of at least one compound according to claim
 1. 11. A method for preventing arteria occlusion following thrombolytic therapy which comprises administering to a patient an effective amount of at least one compound according to claim 1 and an effective amount of at least another antithrombolytic agent.
 12. The method of claim 11 wherein said other antithrombolytic agent is selected from the group consisting of tissue plasminogen activators, streptokinase and urokinase, and functional derivatives thereof.
 13. A method for treating metastatic diseases which comprises administering to a patient an effective amount of at least one compound according to claim
 1. 14. A method of claim 7 which further comprises administering a further anticoagulant agent to said patient.
 15. The method of claim 14 wherein said further anticoagulant agent is selected from the group consisting of heparin, aspirin, and warfarin.
 16. A method for treating a patient in need of an anti-inflammatory agent which comprises administering to said patient an effective amount of at least one of the compounds according to claim
 1. 17. A method for inhibiting in vitro clotting of blood which comprises contacting said blood with at least one compound according to claim
 1. 18. The method of claim 17 which comprises inhibiting said blood in tubes.
 19. An extraarpereal device having a coating therein which comprise a compound according to claim
 1. 20. A method for detecting presence of a serine protease which comprises contacting a sample with a compound according to claim
 1. 21. The compound of claim 1 represented by the structure:

wherein R═CH═CH₂; R₁═H; R₂═CO₂H; R₃═C(O)NHCH₂CH(CH₃)₂; X═CH and

pharmaceutically acceptable salts thereof and prodrugs thereof. 